Canonical Allele Identifier: CA380142153
Gene: RAG2 HGNC NCBI

Linked Data

dbSNP Id: rs1304251505

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36593401G>C , CM000673.2:g.36593401G>C GRCh38
NC_000011.9:g.36614951G>C , CM000673.1:g.36614951G>C GRCh37
NC_000011.8:g.36571527G>C NCBI36
NG_007573.1:g.9836C>G , LRG_99:g.9836C>G
NG_033154.1:g.3909G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000527033.6:c.768C>G ENSP00000436895.2:p.Ile256Met
ENST00000529083.2:c.768C>G ENSP00000436327.2:p.Ile256Met
ENST00000532616.2:c.768C>G ENSP00000432174.2:p.Ile256Met
ENST00000311485.8:c.768C>G MANE Select ENSP00000308620.4:p.Ile256Met
ENST00000311485.7:c.768C>G ENSP00000308620.3:p.Ile256Met
ENST00000524423.1:n.131+4701C>G
ENST00000618712.4:c.768C>G ENSP00000478672.1:p.Ile256Met
NM_000536.3:c.768C>G NP_000527.2:p.Ile256Met
NM_001243785.1:c.768C>G NP_001230714.1:p.Ile256Met
NM_001243786.1:c.768C>G NP_001230715.1:p.Ile256Met
NM_000536.4:c.768C>G MANE Select NP_000527.2:p.Ile256Met
NM_001243785.2:c.768C>G NP_001230714.1:p.Ile256Met
NM_001243786.2:c.768C>G NP_001230715.1:p.Ile256Met