Canonical Allele Identifier: CA2256826679
Gene: ASIC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979488C= , CM000679.2:g.33979488C= GRCh38
NC_000017.10:g.32306507C= , CM000679.1:g.32306507C= GRCh37
NC_000017.9:g.29330620C= NCBI36
NG_029763.1:g.182319G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176490G= ENSP00000352934.6:n.555+176490G=
NM_001094.4:c.555+176490G= NP_001085.2:n.555+176490G=
XR_001752840.1:n.404+7657G=
NM_001094.5:c.555+176490G= NP_001085.2:n.555+176490G=