Canonical Allele Identifier: CA13634871
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.118950113A>C , CM000674.2:g.118950113A>C GRCh38
NC_000012.11:g.119387918A>C , CM000674.1:g.119387918A>C GRCh37
NC_000012.10:g.117872301A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945428.1:n.291-3249T>G
XR_945428.3:n.290-3249T>G