Canonical Allele Identifier: CA289878308

Gene: ASIC2

Linked Data

• dbSNP Id: rs1004039047
• gnomAD v3: 17-33979168-T-A
• gnomAD v4: 17-33979168-T-A
• MyVariant Identifiers: chr17:g.32306187T>A (hg19) ; chr17:g.33979168T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.33979168T>A , CM000679.2:g.33979168T>A	GRCh38
NC_000017.10:g.32306187T>A , CM000679.1:g.32306187T>A	GRCh37
NC_000017.9:g.29330300T>A	NCBI36
NG_029763.1:g.182639A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359872.6:c.555+176810A>T	ENSP00000352934.6:n.555+176810A>T
NM_001094.4:c.555+176810A>T	NP_001085.2:n.555+176810A>T
XR_001752840.1:n.404+7977A>T
NM_001094.5:c.555+176810A>T	NP_001085.2:n.555+176810A>T