Canonical Allele Identifier: CA2776329163
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69147002C>G , CM000669.2:g.69147002C>G GRCh38
NC_000007.13:g.68611989C>G , CM000669.1:g.68611989C>G GRCh37
NC_000007.12:g.68249925C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-876G>C