Canonical Allele Identifier: CA1149397036
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036578T= , CM000663.2:g.2036578T= GRCh38
NC_000001.10:g.1968017T= , CM000663.1:g.1968017T= GRCh37
NC_000001.9:g.1957877T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.630A=
XR_001737845.2:n.633A=
XR_946823.3:n.633A=