Canonical Allele Identifier: CA380140302

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36592704G>C , CM000673.2:g.36592704G>C GRCh38
NC_000011.9:g.36614254G>C , CM000673.1:g.36614254G>C GRCh37
NC_000011.8:g.36570830G>C NCBI36
NG_007573.1:g.10533C>G , LRG_99:g.10533C>G
NG_033154.1:g.3212G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000527033.6:c.1465C>G (RAG2) ENSP00000436895.2:p.His489Asp
ENST00000529083.2:c.1465C>G (RAG2) ENSP00000436327.2:p.His489Asp
ENST00000532616.2:c.1465C>G (RAG2) ENSP00000432174.2:p.His489Asp
ENST00000311485.8:c.1465C>G (RAG2) MANE Select ENSP00000308620.4:p.His489Asp
ENST00000311485.7:c.1465C>G (RAG2) ENSP00000308620.3:p.His489Asp
ENST00000524423.1:n.131+5398C>G (RAG2)
ENST00000534663.1:c.*86-263G>C (RAG1) ENSP00000434610.1:n.*86-263G>C
ENST00000618712.4:c.1465C>G (RAG2) ENSP00000478672.1:p.His489Asp
NM_000536.3:c.1465C>G (RAG2) NP_000527.2:p.His489Asp
NM_001243785.1:c.1465C>G (RAG2) NP_001230714.1:p.His489Asp
NM_001243786.1:c.1465C>G (RAG2) NP_001230715.1:p.His489Asp
NM_000536.4:c.1465C>G (RAG2) MANE Select NP_000527.2:p.His489Asp
NM_001243785.2:c.1465C>G (RAG2) NP_001230714.1:p.His489Asp
NM_001243786.2:c.1465C>G (RAG2) NP_001230715.1:p.His489Asp