Canonical Allele Identifier: CA1222435251
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491656T= , CM000663.2:g.220491656T= GRCh38
NC_000001.10:g.220664998T= , CM000663.1:g.220664998T= GRCh37
NC_000001.9:g.218731621T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922615.1:n.256-578T=
XR_001737822.1:n.557-578T=