Canonical Allele Identifier: CA2566648832
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428232T>C , CM000665.2:g.61428232T>C GRCh38
NC_000003.11:g.61413906T>C , CM000665.1:g.61413906T>C GRCh37
NC_000003.10:g.61388946T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.164+282A>G
XR_940893.1:n.164+282A>G
XR_001740725.1:n.202+282A>G
XR_940892.2:n.202+282A>G