Canonical Allele Identifier: CA728269215

Gene: ASIC2

Linked Data

• dbSNP Id: rs1439778078
• gnomAD v3: 17-33979712-T-C
• gnomAD v4: 17-33979712-T-C
• MyVariant Identifiers: chr17:g.32306731T>C (hg19) ; chr17:g.33979712T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.33979712T>C , CM000679.2:g.33979712T>C	GRCh38
NC_000017.10:g.32306731T>C , CM000679.1:g.32306731T>C	GRCh37
NC_000017.9:g.29330844T>C	NCBI36
NG_029763.1:g.182095A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359872.6:c.555+176266A>G	ENSP00000352934.6:n.555+176266A>G
NM_001094.4:c.555+176266A>G	NP_001085.2:n.555+176266A>G
XR_001752840.1:n.404+7433A>G
NM_001094.5:c.555+176266A>G	NP_001085.2:n.555+176266A>G