Canonical Allele Identifier: CA474033632

Gene: RAG2

Linked Data

• ClinVar Variation Id: 2951678
• ClinVar RCV Id: RCV003812365
• gnomAD v4: 11-36594097-A-G
• MyVariant Identifiers: chr11:g.36615647A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36594097A>G , CM000673.2:g.36594097A>G	GRCh38
NC_000011.9:g.36615647A>G , CM000673.1:g.36615647A>G	GRCh37
NC_000011.8:g.36572223A>G	NCBI36
NG_007573.1:g.9140T>C , LRG_99:g.9140T>C
NG_033154.1:g.4605A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.72T>C	ENSP00000436895.2:p.Phe24=
ENST00000529083.2:c.72T>C	ENSP00000436327.2:p.Phe24=
ENST00000532616.2:c.72T>C	ENSP00000432174.2:p.Phe24=
ENST00000311485.8:c.72T>C MANE Select	ENSP00000308620.4:p.Phe24=
ENST00000311485.7:c.72T>C	ENSP00000308620.3:p.Phe24=
ENST00000524423.1:n.131+4005T>C
ENST00000527033.5:c.72T>C	ENSP00000436895.1:p.Phe24=
ENST00000529083.1:c.72T>C	ENSP00000436327.1:p.Phe24=
ENST00000618712.4:c.72T>C	ENSP00000478672.1:p.Phe24=
NM_000536.3:c.72T>C	NP_000527.2:p.Phe24=
NM_001243785.1:c.72T>C	NP_001230714.1:p.Phe24=
NM_001243786.1:c.72T>C	NP_001230715.1:p.Phe24=
NM_000536.4:c.72T>C MANE Select	NP_000527.2:p.Phe24=
NM_001243785.2:c.72T>C	NP_001230714.1:p.Phe24=
NM_001243786.2:c.72T>C	NP_001230715.1:p.Phe24=