Canonical Allele Identifier: CA2747511294
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454321G>T , CM000663.2:g.207454321G>T GRCh38
NC_000001.10:g.207627666G>T , CM000663.1:g.207627666G>T GRCh37
NC_000001.9:g.205694289G>T NCBI36
NG_013006.1:g.5022G>T , LRG_348:g.5022G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1226G>T ENSP00000514493.1:n.-385+1226G>T
ENST00000367057.7:c.-98G>T ENSP00000356024.3:n.-98G>T
ENST00000367058.7:c.-98G>T ENSP00000356025.3:n.-98G>T
ENST00000367059.3:c.-98G>T ENSP00000356026.3:n.-98G>T
NM_001006658.2:c.-98G>T , LRG_348t1:c.-98G>T NP_001006659.1:n.-98G>T
NM_001877.4:c.-98G>T NP_001868.2:n.-98G>T