Canonical Allele Identifier: CA983177550
Gene: ASIC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979206C>T , CM000679.2:g.33979206C>T GRCh38
NC_000017.10:g.32306225C>T , CM000679.1:g.32306225C>T GRCh37
NC_000017.9:g.29330338C>T NCBI36
NG_029763.1:g.182601G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176772G>A ENSP00000352934.6:n.555+176772G>A
NM_001094.4:c.555+176772G>A NP_001085.2:n.555+176772G>A
XR_001752840.1:n.404+7939G>A
NM_001094.5:c.555+176772G>A NP_001085.2:n.555+176772G>A