Canonical Allele Identifier: CA289769971

Gene: ASIC2

Linked Data

• dbSNP Id: rs992871075
• gnomAD v3: 17-33066789-C-T
• gnomAD v4: 17-33066789-C-T
• MyVariant Identifiers: chr17:g.31393807C>T (hg19) ; chr17:g.33066789C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.33066789C>T , CM000679.2:g.33066789C>T	GRCh38
NC_000017.10:g.31393807C>T , CM000679.1:g.31393807C>T	GRCh37
NC_000017.9:g.28417920C>T	NCBI36
NG_029763.1:g.1095019G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225823.7:c.987+22074G>A MANE Select	ENSP00000225823.2:n.987+22074G>A
ENST00000225823.6:c.987+22074G>A	ENSP00000225823.2:n.987+22074G>A
ENST00000359872.6:c.834+22074G>A	ENSP00000352934.6:n.834+22074G>A
ENST00000448983.1:n.392+22074G>A
NM_001094.4:c.834+22074G>A	NP_001085.2:n.834+22074G>A
NM_183377.1:c.987+22074G>A	NP_899233.1:n.987+22074G>A
NM_001094.5:c.834+22074G>A	NP_001085.2:n.834+22074G>A
NM_183377.2:c.987+22074G>A MANE Select	NP_899233.1:n.987+22074G>A