Canonical Allele Identifier: CA2483404328

Gene: CR2

Linked Data

• dbSNP Id: rs1657745157

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207453864G>C , CM000663.2:g.207453864G>C	GRCh38
NC_000001.10:g.207627209G>C , CM000663.1:g.207627209G>C	GRCh37
NC_000001.9:g.205693832G>C	NCBI36
NG_013006.1:g.4565G>C , LRG_348:g.4565G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699640.1:c.-385+769G>C	ENSP00000514493.1:n.-385+769G>C