Canonical Allele Identifier: CA16271062
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.81483392T>C , CM000668.2:g.81483392T>C GRCh38
NC_000006.11:g.82193109T>C , CM000668.1:g.82193109T>C GRCh37
NC_000006.10:g.82249828T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744218.1:n.1402+8099A>G