Canonical Allele Identifier: CA2483404482
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454185C= , CM000663.2:g.207454185C= GRCh38
NC_000001.10:g.207627530C= , CM000663.1:g.207627530C= GRCh37
NC_000001.9:g.205694153C= NCBI36
NG_013006.1:g.4886C= , LRG_348:g.4886C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1090C= ENSP00000514493.1:n.-385+1090C=