Canonical Allele Identifier: CA2077810922
Community Standard Title: NC_000013.11:g.21619823A=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.21619823A= , CM000675.2:g.21619823A= GRCh38
NC_000013.10:g.22193962A= , CM000675.1:g.22193962A= GRCh37
NC_000013.9:g.21091962A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749772.1:n.321+2650A=
XR_001749773.1:n.321+2650A=