Canonical Allele Identifier: CA625752025
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1253827760

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979456T>G , CM000679.2:g.33979456T>G GRCh38
NC_000017.10:g.32306475T>G , CM000679.1:g.32306475T>G GRCh37
NC_000017.9:g.29330588T>G NCBI36
NG_029763.1:g.182351A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.555+176522A>C ENSP00000352934.6:n.555+176522A>C
NM_001094.4:c.555+176522A>C NP_001085.2:n.555+176522A>C
XR_001752840.1:n.404+7689A>C
NM_001094.5:c.555+176522A>C NP_001085.2:n.555+176522A>C