Canonical Allele Identifier: CA1300258618
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870178A= , CM000664.2:g.155870178A= GRCh38
NC_000002.11:g.156726690A= , CM000664.1:g.156726690A= GRCh37
NC_000002.10:g.156434936A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-2991T=
XR_001739749.1:n.331-29194T=
XR_001739750.1:n.331-29194T=
XR_001739751.1:n.331-29194T=
XR_923501.2:n.331-2991T=