Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs376758084
- Species
- Homo sapiens
- Symbol
- rs376758084
- Category
- Variant
- Variant type
- SNP
- Overlaps
- INHA
- Location
- 2:219575153
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.219575153C>G
- HGVS.c name
- ENSEMBL:ENST00000243786.3:c.728C>G
- RefSeq:NM_002191.4:c.728C>G
- HGVS.p name
- ENSP00000243786:p.Pro243Arg
- NP_002182:p.Pro243Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:219569162...219575711 (6.55 kb)
- Assembly version
- Not Available
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