Canonical Allele Identifier: CA528606447
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1199090736
gnomAD v2: 1-207627579-G-A
gnomAD v3: 1-207454234-G-A
gnomAD v4: 1-207454234-G-A
MyVariant Identifiers: chr1:g.207627579G>A (hg19) chr1:g.207454234G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454234G>A , CM000663.2:g.207454234G>A GRCh38
NC_000001.10:g.207627579G>A , CM000663.1:g.207627579G>A GRCh37
NC_000001.9:g.205694202G>A NCBI36
NG_013006.1:g.4935G>A , LRG_348:g.4935G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1139G>A ENSP00000514493.1:n.-385+1139G>A
ENST00000367057.7:c.-185G>A ENSP00000356024.3:n.-185G>A
ENST00000367058.7:c.-185G>A ENSP00000356025.3:n.-185G>A
ENST00000367059.3:c.-185G>A ENSP00000356026.3:n.-185G>A
Search 100 bp 5'
Search 100 bp 3'