Canonical Allele Identifier: CA1615804282
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.23077034C= , CM000668.2:g.23077034C= GRCh38
NC_000006.11:g.23077262C= , CM000668.1:g.23077262C= GRCh37
NC_000006.10:g.23185241C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926583.1:n.246-19967G=
XR_926584.1:n.246-60214G=
XR_926583.2:n.246-19967G=