Canonical Allele Identifier: CA2483404527
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1657767231

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454246G>A , CM000663.2:g.207454246G>A GRCh38
NC_000001.10:g.207627591G>A , CM000663.1:g.207627591G>A GRCh37
NC_000001.9:g.205694214G>A NCBI36
NG_013006.1:g.4947G>A , LRG_348:g.4947G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1151G>A ENSP00000514493.1:n.-385+1151G>A
ENST00000367057.7:c.-173G>A ENSP00000356024.3:n.-173G>A
ENST00000367058.7:c.-173G>A ENSP00000356025.3:n.-173G>A
ENST00000367059.3:c.-173G>A ENSP00000356026.3:n.-173G>A