Canonical Allele Identifier: CA2650261324

Gene: CR2

Linked Data

• gnomAD v4: 1-207454326-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454326A>C , CM000663.2:g.207454326A>C	GRCh38
NC_000001.10:g.207627671A>C , CM000663.1:g.207627671A>C	GRCh37
NC_000001.9:g.205694294A>C	NCBI36
NG_013006.1:g.5027A>C , LRG_348:g.5027A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699640.1:c.-385+1231A>C	ENSP00000514493.1:n.-385+1231A>C
ENST00000367057.7:c.-93A>C	ENSP00000356024.3:n.-93A>C
ENST00000367058.7:c.-93A>C	ENSP00000356025.3:n.-93A>C
ENST00000367059.3:c.-93A>C	ENSP00000356026.3:n.-93A>C
NM_001006658.2:c.-93A>C , LRG_348t1:c.-93A>C	NP_001006659.1:n.-93A>C
NM_001877.4:c.-93A>C	NP_001868.2:n.-93A>C