Canonical Allele Identifier: CA2572641896
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453911G>T , CM000663.2:g.207453911G>T GRCh38
NC_000001.10:g.207627256G>T , CM000663.1:g.207627256G>T GRCh37
NC_000001.9:g.205693879G>T NCBI36
NG_013006.1:g.4612G>T , LRG_348:g.4612G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+816G>T ENSP00000514493.1:n.-385+816G>T