Canonical Allele Identifier: CA1769538729
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20768805G= , CM000670.2:g.20768805G= GRCh38
NC_000008.10:g.20626316G= , CM000670.1:g.20626316G= GRCh37
NC_000008.9:g.20670596G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949569.3:n.72-21641G=