Canonical Allele Identifier: CA1205766010
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649416T= , CM000663.2:g.168649416T= GRCh38
NC_000001.10:g.168618654T= , CM000663.1:g.168618654T= GRCh37
NC_000001.9:g.166885278T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8141A=
XR_922259.2:n.332-8141A=