Canonical Allele Identifier: CA2650261094
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454151G>C , CM000663.2:g.207454151G>C GRCh38
NC_000001.10:g.207627496G>C , CM000663.1:g.207627496G>C GRCh37
NC_000001.9:g.205694119G>C NCBI36
NG_013006.1:g.4852G>C , LRG_348:g.4852G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1056G>C ENSP00000514493.1:n.-385+1056G>C