Canonical Allele Identifier: CA2841795926
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146856A>C , CM000669.2:g.69146856A>C GRCh38
NC_000007.13:g.68611843A>C , CM000669.1:g.68611843A>C GRCh37
NC_000007.12:g.68249779A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927647.1:n.88-730T>G