Canonical Allele Identifier: CA1149397021
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036559C= , CM000663.2:g.2036559C= GRCh38
NC_000001.10:g.1967998C= , CM000663.1:g.1967998C= GRCh37
NC_000001.9:g.1957858C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.649G=
XR_001737845.2:n.652G=
XR_946823.3:n.652G=