Canonical Allele Identifier: CA1223909893
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068546T= , CM000663.2:g.224068546T= GRCh38
NC_000001.10:g.224256248T= , CM000663.1:g.224256248T= GRCh37
NC_000001.9:g.222322871T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+892T=
XR_001737824.1:n.242+892T=