Canonical Allele Identifier: CA2592948139
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs2142003042

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979287A>G , CM000679.2:g.33979287A>G GRCh38
NC_000017.10:g.32306306A>G , CM000679.1:g.32306306A>G GRCh37
NC_000017.9:g.29330419A>G NCBI36
NG_029763.1:g.182520T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176691T>C ENSP00000352934.6:n.555+176691T>C
NM_001094.4:c.555+176691T>C NP_001085.2:n.555+176691T>C
XR_001752840.1:n.404+7858T>C
NM_001094.5:c.555+176691T>C NP_001085.2:n.555+176691T>C