Canonical Allele Identifier: CA1989925820
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89157946A>T , CM000673.2:g.89157946A>T GRCh38
NC_000011.9:g.88891114A>T , CM000673.1:g.88891114A>T GRCh37
NC_000011.8:g.88530762A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748321.1:n.2718-44413T>A
XR_001748322.1:n.2733-44413T>A