Canonical Allele Identifier: CA1149396957
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036480C= , CM000663.2:g.2036480C= GRCh38
NC_000001.10:g.1967919C= , CM000663.1:g.1967919C= GRCh37
NC_000001.9:g.1957779C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.728G=
XR_001737845.2:n.731G=
XR_946823.3:n.731G=