Canonical Allele Identifier: CA13003168
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134532196G>A , CM000671.2:g.134532196G>A GRCh38
NC_000009.11:g.137424042G>A , CM000671.1:g.137424042G>A GRCh37
NC_000009.10:g.136563863G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_109854.3:n.2567+4912G>A
XR_930416.1:n.171-12724G>A
XR_930417.1:n.342-12724G>A
XR_109854.5:n.2496+4912G>A
XR_930416.2:n.194-12724G>A
XR_930417.2:n.365-12724G>A