Canonical Allele Identifier: CA14448139
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs317332

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979308A>G , CM000679.2:g.33979308A>G GRCh38
NC_000017.10:g.32306327A>G , CM000679.1:g.32306327A>G GRCh37
NC_000017.9:g.29330440A>G NCBI36
NG_029763.1:g.182499T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176670T>C ENSP00000352934.6:n.555+176670T>C
NM_001094.4:c.555+176670T>C NP_001085.2:n.555+176670T>C
XR_001752840.1:n.404+7837T>C
NM_001094.5:c.555+176670T>C NP_001085.2:n.555+176670T>C