Canonical Allele Identifier: CA2776329165
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69147044G>T , CM000669.2:g.69147044G>T GRCh38
NC_000007.13:g.68612031G>T , CM000669.1:g.68612031G>T GRCh37
NC_000007.12:g.68249967G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-918C>A