Canonical Allele Identifier: CA1688067907
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.11251773G= , CM000669.2:g.11251773G= GRCh38
NC_000007.13:g.11291400G= , CM000669.1:g.11291400G= GRCh37
NC_000007.12:g.11257925G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744902.2:n.3392G=