Canonical Allele Identifier: CA14447916
Gene: ASIC2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17808461

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33066684C>T , CM000679.2:g.33066684C>T GRCh38
NC_000017.9:g.28417815C>T NCBI36
NC_000017.10:g.31393702C>T , CM000679.1:g.31393702C>T GRCh37
NG_029763.1:g.1095124G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225823.6:c.987+22179G>A ENSP00000225823.2:p.=
ENST00000359872.6:c.834+22179G>A ENSP00000352934.6:p.=
ENST00000448983.1:n.392+22179G>A
NM_001094.4:c.834+22179G>A NP_001085.2:p.=
NM_183377.1:c.987+22179G>A NP_899233.1:p.=