Canonical Allele Identifier: CA289878339

Gene: ASIC2

Linked Data

• dbSNP Id: rs905363853
• gnomAD v3: 17-33979429-C-A
• gnomAD v4: 17-33979429-C-A
• MyVariant Identifiers: chr17:g.32306448C>A (hg19) ; chr17:g.33979429C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.33979429C>A , CM000679.2:g.33979429C>A	GRCh38
NC_000017.10:g.32306448C>A , CM000679.1:g.32306448C>A	GRCh37
NC_000017.9:g.29330561C>A	NCBI36
NG_029763.1:g.182378G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359872.6:c.555+176549G>T	ENSP00000352934.6:n.555+176549G>T
NM_001094.4:c.555+176549G>T	NP_001085.2:n.555+176549G>T
XR_001752840.1:n.404+7716G>T
NM_001094.5:c.555+176549G>T	NP_001085.2:n.555+176549G>T