Canonical Allele Identifier: CA2256826680
Gene: ASIC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979489A= , CM000679.2:g.33979489A= GRCh38
NC_000017.10:g.32306508A= , CM000679.1:g.32306508A= GRCh37
NC_000017.9:g.29330621A= NCBI36
NG_029763.1:g.182318T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176489T= ENSP00000352934.6:n.555+176489T=
NM_001094.4:c.555+176489T= NP_001085.2:n.555+176489T=
XR_001752840.1:n.404+7656T=
NM_001094.5:c.555+176489T= NP_001085.2:n.555+176489T=