Canonical Allele Identifier: CA2650261306
Gene: CR2 HGNC NCBI

Linked Data

gnomAD v4: 1-207454309-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454309C>T , CM000663.2:g.207454309C>T GRCh38
NC_000001.10:g.207627654C>T , CM000663.1:g.207627654C>T GRCh37
NC_000001.9:g.205694277C>T NCBI36
NG_013006.1:g.5010C>T , LRG_348:g.5010C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1214C>T ENSP00000514493.1:n.-385+1214C>T
ENST00000367057.7:c.-110C>T ENSP00000356024.3:n.-110C>T
ENST00000367058.7:c.-110C>T ENSP00000356025.3:n.-110C>T
ENST00000367059.3:c.-110C>T ENSP00000356026.3:n.-110C>T
NM_001006658.2:c.-110C>T , LRG_348t1:c.-110C>T NP_001006659.1:n.-110C>T
NM_001877.4:c.-110C>T NP_001868.2:n.-110C>T
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