Canonical Allele Identifier: CA983177746
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1905538535

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979633C>T , CM000679.2:g.33979633C>T GRCh38
NC_000017.10:g.32306652C>T , CM000679.1:g.32306652C>T GRCh37
NC_000017.9:g.29330765C>T NCBI36
NG_029763.1:g.182174G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176345G>A ENSP00000352934.6:n.555+176345G>A
NM_001094.4:c.555+176345G>A NP_001085.2:n.555+176345G>A
XR_001752840.1:n.404+7512G>A
NM_001094.5:c.555+176345G>A NP_001085.2:n.555+176345G>A