Canonical Allele Identifier: CA1267947594
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016372G= , CM000664.2:g.88016372G= GRCh38
NC_000002.11:g.88315891G= , CM000664.1:g.88315891G= GRCh37
NC_000002.10:g.88097006G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.717G=
XR_940336.3:n.717G=