Canonical Allele Identifier: CA1912720921
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812900C= , CM000672.2:g.57812900C= GRCh38
NC_000010.10:g.59572660C= , CM000672.1:g.59572660C= GRCh37
NC_000010.9:g.59242666C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34392G=
XR_001747454.1:n.85+34392G=