Canonical Allele Identifier: CA2798028863
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529672A>C , CM000674.2:g.131529672A>C GRCh38
NC_000012.11:g.132014217A>C , CM000674.1:g.132014217A>C GRCh37
NC_000012.10:g.130580170A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+103T>G
XR_001749407.2:n.1067+103T>G