Canonical Allele Identifier: CA1267947549
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016341G= , CM000664.2:g.88016341G= GRCh38
NC_000002.11:g.88315860G= , CM000664.1:g.88315860G= GRCh37
NC_000002.10:g.88096975G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.686G=
XR_940336.3:n.686G=