Canonical Allele Identifier: CA380144742

Gene: RAG2

Linked Data

• MyVariant Identifiers: chr11:g.36615633A>G (hg19) ; chr11:g.36594083A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36594083A>G , CM000673.2:g.36594083A>G	GRCh38
NC_000011.9:g.36615633A>G , CM000673.1:g.36615633A>G	GRCh37
NC_000011.8:g.36572209A>G	NCBI36
NG_007573.1:g.9154T>C , LRG_99:g.9154T>C
NG_033154.1:g.4591A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.86T>C	ENSP00000436895.2:p.Phe29Ser
ENST00000529083.2:c.86T>C	ENSP00000436327.2:p.Phe29Ser
ENST00000532616.2:c.86T>C	ENSP00000432174.2:p.Phe29Ser
ENST00000311485.8:c.86T>C MANE Select	ENSP00000308620.4:p.Phe29Ser
ENST00000311485.7:c.86T>C	ENSP00000308620.3:p.Phe29Ser
ENST00000524423.1:n.131+4019T>C
ENST00000527033.5:c.86T>C	ENSP00000436895.1:p.Phe29Ser
ENST00000529083.1:c.86T>C	ENSP00000436327.1:p.Phe29Ser
ENST00000618712.4:c.86T>C	ENSP00000478672.1:p.Phe29Ser
NM_000536.3:c.86T>C	NP_000527.2:p.Phe29Ser
NM_001243785.1:c.86T>C	NP_001230714.1:p.Phe29Ser
NM_001243786.1:c.86T>C	NP_001230715.1:p.Phe29Ser
NM_000536.4:c.86T>C MANE Select	NP_000527.2:p.Phe29Ser
NM_001243785.2:c.86T>C	NP_001230714.1:p.Phe29Ser
NM_001243786.2:c.86T>C	NP_001230715.1:p.Phe29Ser