Canonical Allele Identifier: CA2650261132
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454186C>T , CM000663.2:g.207454186C>T GRCh38
NC_000001.10:g.207627531C>T , CM000663.1:g.207627531C>T GRCh37
NC_000001.9:g.205694154C>T NCBI36
NG_013006.1:g.4887C>T , LRG_348:g.4887C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1091C>T ENSP00000514493.1:n.-385+1091C>T