Canonical Allele Identifier: CA1149396959
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036481C= , CM000663.2:g.2036481C= GRCh38
NC_000001.10:g.1967920C= , CM000663.1:g.1967920C= GRCh37
NC_000001.9:g.1957780C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.727G=
XR_001737845.2:n.730G=
XR_946823.3:n.730G=