Canonical Allele Identifier: CA1267947359
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016179G= , CM000664.2:g.88016179G= GRCh38
NC_000002.11:g.88315698G= , CM000664.1:g.88315698G= GRCh37
NC_000002.10:g.88096813G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.524G=
XR_940336.3:n.524G=