Canonical Allele Identifier: CA1964194686
Gene: RAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36593408C= , CM000673.2:g.36593408C= GRCh38
NC_000011.9:g.36614958C= , CM000673.1:g.36614958C= GRCh37
NC_000011.8:g.36571534C= NCBI36
NG_007573.1:g.9829G= , LRG_99:g.9829G=
NG_033154.1:g.3916C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000527033.6:c.761G= ENSP00000436895.2:p.Gly254=
ENST00000529083.2:c.761G= ENSP00000436327.2:p.Gly254=
ENST00000532616.2:c.761G= ENSP00000432174.2:p.Gly254=
ENST00000311485.8:c.761G= MANE Select ENSP00000308620.4:p.Gly254=
ENST00000311485.7:c.761G= ENSP00000308620.3:p.Gly254=
ENST00000524423.1:n.131+4694G=
ENST00000618712.4:c.761G= ENSP00000478672.1:p.Gly254=
NM_000536.3:c.761G= NP_000527.2:p.Gly254=
NM_001243785.1:c.761G= NP_001230714.1:p.Gly254=
NM_001243786.1:c.761G= NP_001230715.1:p.Gly254=
NM_000536.4:c.761G= MANE Select NP_000527.2:p.Gly254=
NM_001243785.2:c.761G= NP_001230714.1:p.Gly254=
NM_001243786.2:c.761G= NP_001230715.1:p.Gly254=