Canonical Allele Identifier: CA1964196376
Gene: RAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36593965G= , CM000673.2:g.36593965G= GRCh38
NC_000011.9:g.36615515G= , CM000673.1:g.36615515G= GRCh37
NC_000011.8:g.36572091G= NCBI36
NG_007573.1:g.9272C= , LRG_99:g.9272C=
NG_033154.1:g.4473G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000527033.6:c.204C= ENSP00000436895.2:p.Tyr68=
ENST00000529083.2:c.204C= ENSP00000436327.2:p.Tyr68=
ENST00000532616.2:c.204C= ENSP00000432174.2:p.Tyr68=
ENST00000311485.8:c.204C= MANE Select ENSP00000308620.4:p.Tyr68=
ENST00000311485.7:c.204C= ENSP00000308620.3:p.Tyr68=
ENST00000524423.1:n.131+4137C=
ENST00000527033.5:c.204C= ENSP00000436895.1:p.Tyr68=
ENST00000529083.1:c.204C= ENSP00000436327.1:p.Tyr68=
ENST00000618712.4:c.204C= ENSP00000478672.1:p.Tyr68=
NM_000536.3:c.204C= NP_000527.2:p.Tyr68=
NM_001243785.1:c.204C= NP_001230714.1:p.Tyr68=
NM_001243786.1:c.204C= NP_001230715.1:p.Tyr68=
NM_000536.4:c.204C= MANE Select NP_000527.2:p.Tyr68=
NM_001243785.2:c.204C= NP_001230714.1:p.Tyr68=
NM_001243786.2:c.204C= NP_001230715.1:p.Tyr68=