Canonical Allele Identifier: CA1957110175
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.21647747G= , CM000673.2:g.21647747G= GRCh38
NC_000011.9:g.21669293G= , CM000673.1:g.21669293G= GRCh37
NC_000011.8:g.21625869G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748150.1:n.585C=