Canonical Allele Identifier: CA728145995

Gene: ASIC2

Linked Data

• dbSNP Id: rs919670089
• MyVariant Identifiers: chr17:g.31393795T>A (hg19) ; chr17:g.33066777T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.33066777T>A , CM000679.2:g.33066777T>A	GRCh38
NC_000017.10:g.31393795T>A , CM000679.1:g.31393795T>A	GRCh37
NC_000017.9:g.28417908T>A	NCBI36
NG_029763.1:g.1095031A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225823.7:c.987+22086A>T MANE Select	ENSP00000225823.2:n.987+22086A>T
ENST00000225823.6:c.987+22086A>T	ENSP00000225823.2:n.987+22086A>T
ENST00000359872.6:c.834+22086A>T	ENSP00000352934.6:n.834+22086A>T
ENST00000448983.1:n.392+22086A>T
NM_001094.4:c.834+22086A>T	NP_001085.2:n.834+22086A>T
NM_183377.1:c.987+22086A>T	NP_899233.1:n.987+22086A>T
NM_001094.5:c.834+22086A>T	NP_001085.2:n.834+22086A>T
NM_183377.2:c.987+22086A>T MANE Select	NP_899233.1:n.987+22086A>T