Canonical Allele Identifier: CA1687324649
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.9816880C= , CM000669.2:g.9816880C= GRCh38
NC_000007.13:g.9856509C= , CM000669.1:g.9856509C= GRCh37
NC_000007.12:g.9823034C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927024.1:n.209+49910G=
XR_927025.1:n.323+49910G=
XR_927026.1:n.209+49910G=
XR_927026.2:n.209+49910G=