Canonical Allele Identifier: CA1300258802
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870611T= , CM000664.2:g.155870611T= GRCh38
NC_000002.11:g.156727123T= , CM000664.1:g.156727123T= GRCh37
NC_000002.10:g.156435369T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3424A=
XR_001739749.1:n.331-29627A=
XR_001739750.1:n.331-29627A=
XR_001739751.1:n.331-29627A=
XR_923501.2:n.331-3424A=