Canonical Allele Identifier: CA1964195304
Gene: RAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36593556A= , CM000673.2:g.36593556A= GRCh38
NC_000011.9:g.36615106A= , CM000673.1:g.36615106A= GRCh37
NC_000011.8:g.36571682A= NCBI36
NG_007573.1:g.9681T= , LRG_99:g.9681T=
NG_033154.1:g.4064A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000527033.6:c.613T= ENSP00000436895.2:p.Ser205=
ENST00000529083.2:c.613T= ENSP00000436327.2:p.Ser205=
ENST00000532616.2:c.613T= ENSP00000432174.2:p.Ser205=
ENST00000311485.8:c.613T= MANE Select ENSP00000308620.4:p.Ser205=
ENST00000311485.7:c.613T= ENSP00000308620.3:p.Ser205=
ENST00000524423.1:n.131+4546T=
ENST00000618712.4:c.613T= ENSP00000478672.1:p.Ser205=
NM_000536.3:c.613T= NP_000527.2:p.Ser205=
NM_001243785.1:c.613T= NP_001230714.1:p.Ser205=
NM_001243786.1:c.613T= NP_001230715.1:p.Ser205=
NM_000536.4:c.613T= MANE Select NP_000527.2:p.Ser205=
NM_001243785.2:c.613T= NP_001230714.1:p.Ser205=
NM_001243786.2:c.613T= NP_001230715.1:p.Ser205=