Canonical Allele Identifier: CA1706591902
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50409455C= , CM000669.2:g.50409455C= GRCh38
NC_000007.13:g.50477153C= , CM000669.1:g.50477153C= GRCh37
NC_000007.12:g.50444647C= NCBI36