Canonical Allele Identifier: CA1912720956
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812988T= , CM000672.2:g.57812988T= GRCh38
NC_000010.10:g.59572748T= , CM000672.1:g.59572748T= GRCh37
NC_000010.9:g.59242754T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34304A=
XR_001747454.1:n.85+34304A=