Canonical Allele Identifier: CA2650261245
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454256C>A , CM000663.2:g.207454256C>A GRCh38
NC_000001.10:g.207627601C>A , CM000663.1:g.207627601C>A GRCh37
NC_000001.9:g.205694224C>A NCBI36
NG_013006.1:g.4957C>A , LRG_348:g.4957C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000699640.1:c.-385+1161C>A ENSP00000514493.1:n.-385+1161C>A
ENST00000367057.7:c.-163C>A ENSP00000356024.3:n.-163C>A
ENST00000367058.7:c.-163C>A ENSP00000356025.3:n.-163C>A
ENST00000367059.3:c.-163C>A ENSP00000356026.3:n.-163C>A