Canonical Allele Identifier: CA2755699292
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30420860T>G , CM000665.2:g.30420860T>G GRCh38
NC_000003.11:g.30462352T>G , CM000665.1:g.30462352T>G GRCh37
NC_000003.10:g.30437356T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940686.1:n.1367+28972T>G
XR_940687.1:n.1415+28972T>G
XR_001740627.1:n.801+28972T>G
XR_001740628.1:n.849+28972T>G
XR_427322.3:n.802-15333T>G
XR_940683.2:n.1800A>C