Canonical Allele Identifier: CA289878370

Gene: ASIC2

Linked Data

• dbSNP Id: rs565057650
• gnomAD v3: 17-33979706-T-G
• gnomAD v4: 17-33979706-T-G
• MyVariant Identifiers: chr17:g.32306725T>G (hg19) ; chr17:g.33979706T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.33979706T>G , CM000679.2:g.33979706T>G	GRCh38
NC_000017.10:g.32306725T>G , CM000679.1:g.32306725T>G	GRCh37
NC_000017.9:g.29330838T>G	NCBI36
NG_029763.1:g.182101A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359872.6:c.555+176272A>C	ENSP00000352934.6:n.555+176272A>C
NM_001094.4:c.555+176272A>C	NP_001085.2:n.555+176272A>C
XR_001752840.1:n.404+7439A>C
NM_001094.5:c.555+176272A>C	NP_001085.2:n.555+176272A>C