Canonical Allele Identifier: CA2650261331

Gene: CR2

Linked Data

• gnomAD v4: 1-207454332-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454332G>T , CM000663.2:g.207454332G>T	GRCh38
NC_000001.10:g.207627677G>T , CM000663.1:g.207627677G>T	GRCh37
NC_000001.9:g.205694300G>T	NCBI36
NG_013006.1:g.5033G>T , LRG_348:g.5033G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699640.1:c.-385+1237G>T	ENSP00000514493.1:n.-385+1237G>T
ENST00000367057.8:c.-87G>T MANE Select	ENSP00000356024.3:n.-87G>T
ENST00000367057.7:c.-87G>T	ENSP00000356024.3:n.-87G>T
ENST00000367058.7:c.-87G>T	ENSP00000356025.3:n.-87G>T
ENST00000367059.3:c.-87G>T	ENSP00000356026.3:n.-87G>T
NM_001006658.2:c.-87G>T , LRG_348t1:c.-87G>T	NP_001006659.1:n.-87G>T
NM_001877.4:c.-87G>T	NP_001868.2:n.-87G>T
NM_001006658.3:c.-87G>T MANE Select	NP_001006659.1:n.-87G>T
NM_001877.5:c.-87G>T	NP_001868.2:n.-87G>T