Canonical Allele Identifier: CA730645843
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1381261811
gnomAD v3: 1-207454247-C-T
gnomAD v4: 1-207454247-C-T
MyVariant Identifiers: chr1:g.207627592C>T (hg19) chr1:g.207454247C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454247C>T , CM000663.2:g.207454247C>T GRCh38
NC_000001.10:g.207627592C>T , CM000663.1:g.207627592C>T GRCh37
NC_000001.9:g.205694215C>T NCBI36
NG_013006.1:g.4948C>T , LRG_348:g.4948C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1152C>T ENSP00000514493.1:n.-385+1152C>T
ENST00000367057.7:c.-172C>T ENSP00000356024.3:n.-172C>T
ENST00000367058.7:c.-172C>T ENSP00000356025.3:n.-172C>T
ENST00000367059.3:c.-172C>T ENSP00000356026.3:n.-172C>T
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