Canonical Allele Identifier: CA1300258766
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870540T= , CM000664.2:g.155870540T= GRCh38
NC_000002.11:g.156727052T= , CM000664.1:g.156727052T= GRCh37
NC_000002.10:g.156435298T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3353A=
XR_001739749.1:n.331-29556A=
XR_001739750.1:n.331-29556A=
XR_001739751.1:n.331-29556A=
XR_923501.2:n.331-3353A=