Canonical Allele Identifier: CA1912720769
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812605C= , CM000672.2:g.57812605C= GRCh38
NC_000010.10:g.59572365C= , CM000672.1:g.59572365C= GRCh37
NC_000010.9:g.59242371C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34687G=
XR_001747454.1:n.85+34687G=