Canonical Allele Identifier: CA1144976164
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036560T= , CM000663.2:g.2036560T= GRCh38
NC_000001.10:g.1967999T= , CM000663.1:g.1967999T= GRCh37
NC_000001.9:g.1957859T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.648A=
XR_001737845.2:n.651A=
XR_946823.3:n.651A=