Canonical Allele Identifier: CA2650261192
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454216G>A , CM000663.2:g.207454216G>A GRCh38
NC_000001.10:g.207627561G>A , CM000663.1:g.207627561G>A GRCh37
NC_000001.9:g.205694184G>A NCBI36
NG_013006.1:g.4917G>A , LRG_348:g.4917G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1121G>A ENSP00000514493.1:n.-385+1121G>A