Canonical Allele Identifier: CA983177645
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1905521560

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979348G>A , CM000679.2:g.33979348G>A GRCh38
NC_000017.10:g.32306367G>A , CM000679.1:g.32306367G>A GRCh37
NC_000017.9:g.29330480G>A NCBI36
NG_029763.1:g.182459C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176630C>T ENSP00000352934.6:n.555+176630C>T
NM_001094.4:c.555+176630C>T NP_001085.2:n.555+176630C>T
XR_001752840.1:n.404+7797C>T
NM_001094.5:c.555+176630C>T NP_001085.2:n.555+176630C>T