Canonical Allele Identifier: CA1149397008
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036539C= , CM000663.2:g.2036539C= GRCh38
NC_000001.10:g.1967978C= , CM000663.1:g.1967978C= GRCh37
NC_000001.9:g.1957838C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.669G=
XR_001737845.2:n.672G=
XR_946823.3:n.672G=