Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs772177439
- Species
- Homo sapiens
- Symbol
- rs772177439
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MSTN
- Location
- 2:190057274
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000002.12:g.190057274C>T
- HGVS.c name
- ENSEMBL:ENST00000260950.5:c.1112G>A
- ENSEMBL:ENST00000478197.1:n.220-21949C>T
- HGVS.p name
- ENSP00000260950:p.Arg371His
- NP_005250:p.Arg371His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:190055700...190062729 (7.03 kb)
- Assembly version
- Not Available
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