Canonical Allele Identifier: CA1223909916
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068616G= , CM000663.2:g.224068616G= GRCh38
NC_000001.10:g.224256318G= , CM000663.1:g.224256318G= GRCh37
NC_000001.9:g.222322941G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+962G=
XR_001737824.1:n.242+962G=