Canonical Allele Identifier: CA1011643119
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1657752836

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454060C>T , CM000663.2:g.207454060C>T GRCh38
NC_000001.10:g.207627405C>T , CM000663.1:g.207627405C>T GRCh37
NC_000001.9:g.205694028C>T NCBI36
NG_013006.1:g.4761C>T , LRG_348:g.4761C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+965C>T ENSP00000514493.1:n.-385+965C>T