rs746904695

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Species

Homo sapiens

Symbol

rs746904695

Category

Variant

Variant type

SNP

Overlaps

INHA

Location

2:219574904

Nucleotide Change

G>C

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)2:219574904G>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000243786.3:c.479G>C
• ENSEMBL:ENST00000489456.1:n.496G>C

Show All 3

HGVS.p name

• ENSP00000243786:p.Gly160Ala
• NP_002182:p.Gly160Ala

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences