Canonical Allele Identifier: CA2834927872
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146978C>A , CM000669.2:g.69146978C>A GRCh38
NC_000007.13:g.68611965C>A , CM000669.1:g.68611965C>A GRCh37
NC_000007.12:g.68249901C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927647.1:n.88-852G>T