Canonical Allele Identifier: CA1267947608
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016391A= , CM000664.2:g.88016391A= GRCh38
NC_000002.11:g.88315910A= , CM000664.1:g.88315910A= GRCh37
NC_000002.10:g.88097025A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.736A=
XR_940336.3:n.736A=