Canonical Allele Identifier: CA11638432
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.13100727G>T , CM000666.2:g.13100727G>T GRCh38
NC_000004.11:g.13102351G>T , CM000666.1:g.13102351G>T GRCh37
NC_000004.10:g.12711449G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925410.1:n.456+45805C>A