Canonical Allele Identifier: CA1912720788
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812652C= , CM000672.2:g.57812652C= GRCh38
NC_000010.10:g.59572412C= , CM000672.1:g.59572412C= GRCh37
NC_000010.9:g.59242418C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34640G=
XR_001747454.1:n.85+34640G=