Canonical Allele Identifier: CA1222435235
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491635T= , CM000663.2:g.220491635T= GRCh38
NC_000001.10:g.220664977T= , CM000663.1:g.220664977T= GRCh37
NC_000001.9:g.218731600T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922615.1:n.256-599T=
XR_001737822.1:n.557-599T=