Canonical Allele Identifier: CA1563985363
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93151837T>G , CM000667.2:g.93151837T>G GRCh38
NC_000005.9:g.92487543T>G , CM000667.1:g.92487543T>G GRCh37
NC_000005.8:g.92513299T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948569.1:n.130-1931A>C
XR_948569.2:n.197-1931A>C