Canonical Allele Identifier: CA1912720922
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812901C= , CM000672.2:g.57812901C= GRCh38
NC_000010.10:g.59572661C= , CM000672.1:g.59572661C= GRCh37
NC_000010.9:g.59242667C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34391G=
XR_001747454.1:n.85+34391G=