Canonical Allele Identifier: CA983177665
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1905525619

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979418C>A , CM000679.2:g.33979418C>A GRCh38
NC_000017.10:g.32306437C>A , CM000679.1:g.32306437C>A GRCh37
NC_000017.9:g.29330550C>A NCBI36
NG_029763.1:g.182389G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176560G>T ENSP00000352934.6:n.555+176560G>T
NM_001094.4:c.555+176560G>T NP_001085.2:n.555+176560G>T
XR_001752840.1:n.404+7727G>T
NM_001094.5:c.555+176560G>T NP_001085.2:n.555+176560G>T