Canonical Allele Identifier: CA1989925818
Gene:

Genomic Alleles

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

Transcript Alleles

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