Canonical Allele Identifier: CA5950415

Gene: RAG2 RAG1

Linked Data

• ClinVar Variation Id: 2935560
• ClinVar RCV Id: RCV003793654
• dbSNP Id: rs762054841
• ExAC: 11:36614278 G / C
• gnomAD v2: 11-36614278-G-C
• gnomAD v4: 11-36592728-G-C
• MyVariant Identifiers: chr11:g.36614278G>C (hg19) ; chr11:g.36592728G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36592728G>C , CM000673.2:g.36592728G>C	GRCh38
NC_000011.9:g.36614278G>C , CM000673.1:g.36614278G>C	GRCh37
NC_000011.8:g.36570854G>C	NCBI36
NG_007573.1:g.10509C>G , LRG_99:g.10509C>G
NG_033154.1:g.3236G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.1441C>G (RAG2)	ENSP00000436895.2:p.His481Asp
ENST00000529083.2:c.1441C>G (RAG2)	ENSP00000436327.2:p.His481Asp
ENST00000532616.2:c.1441C>G (RAG2)	ENSP00000432174.2:p.His481Asp
ENST00000311485.8:c.1441C>G (RAG2) MANE Select	ENSP00000308620.4:p.His481Asp
ENST00000311485.7:c.1441C>G (RAG2)	ENSP00000308620.3:p.His481Asp
ENST00000524423.1:n.131+5374C>G (RAG2)
ENST00000534663.1:c.*86-239G>C (RAG1)	ENSP00000434610.1:n.*86-239G>C
ENST00000618712.4:c.1441C>G (RAG2)	ENSP00000478672.1:p.His481Asp
NM_000536.3:c.1441C>G (RAG2)	NP_000527.2:p.His481Asp
NM_001243785.1:c.1441C>G (RAG2)	NP_001230714.1:p.His481Asp
NM_001243786.1:c.1441C>G (RAG2)	NP_001230715.1:p.His481Asp
NM_000536.4:c.1441C>G (RAG2) MANE Select	NP_000527.2:p.His481Asp
NM_001243785.2:c.1441C>G (RAG2)	NP_001230714.1:p.His481Asp
NM_001243786.2:c.1441C>G (RAG2)	NP_001230715.1:p.His481Asp