Canonical Allele Identifier: CA422954852
Gene: CR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.207627737T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454392T>A , CM000663.2:g.207454392T>A GRCh38
NC_000001.10:g.207627737T>A , CM000663.1:g.207627737T>A GRCh37
NC_000001.9:g.205694360T>A NCBI36
NG_013006.1:g.5093T>A , LRG_348:g.5093T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699620.1:c.-469T>A ENSP00000514480.1:n.-469T>A
ENST00000699640.1:c.-385+1297T>A ENSP00000514493.1:n.-385+1297T>A
ENST00000367057.8:c.-27T>A MANE Select ENSP00000356024.3:n.-27T>A
ENST00000367057.7:c.-27T>A ENSP00000356024.3:n.-27T>A
ENST00000367058.7:c.-27T>A ENSP00000356025.3:n.-27T>A
ENST00000367059.3:c.-27T>A ENSP00000356026.3:n.-27T>A
NM_001006658.2:c.-27T>A , LRG_348t1:c.-27T>A NP_001006659.1:n.-27T>A
NM_001877.4:c.-27T>A NP_001868.2:n.-27T>A
NM_001006658.3:c.-27T>A MANE Select NP_001006659.1:n.-27T>A
NM_001877.5:c.-27T>A NP_001868.2:n.-27T>A
Search 100 bp 5'
Search 100 bp 3'