Canonical Allele Identifier: CA36637642
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs919219552

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454251C>T , CM000663.2:g.207454251C>T GRCh38
NC_000001.10:g.207627596C>T , CM000663.1:g.207627596C>T GRCh37
NC_000001.9:g.205694219C>T NCBI36
NG_013006.1:g.4952C>T , LRG_348:g.4952C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000699640.1:c.-385+1156C>T ENSP00000514493.1:n.-385+1156C>T
ENST00000367057.7:c.-168C>T ENSP00000356024.3:n.-168C>T
ENST00000367058.7:c.-168C>T ENSP00000356025.3:n.-168C>T
ENST00000367059.3:c.-168C>T ENSP00000356026.3:n.-168C>T