Canonical Allele Identifier: CA2256826670
Gene: ASIC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979465T= , CM000679.2:g.33979465T= GRCh38
NC_000017.10:g.32306484T= , CM000679.1:g.32306484T= GRCh37
NC_000017.9:g.29330597T= NCBI36
NG_029763.1:g.182342A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176513A= ENSP00000352934.6:n.555+176513A=
NM_001094.4:c.555+176513A= NP_001085.2:n.555+176513A=
XR_001752840.1:n.404+7680A=
NM_001094.5:c.555+176513A= NP_001085.2:n.555+176513A=