gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136925969G>C , CM000671.2:g.136925969G>C | GRCh38 |
| NC_000009.11:g.139820421G>C , CM000671.1:g.139820421G>C | GRCh37 |
| NC_000009.10:g.138940242G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000247668.7:c.*68G>C (TRAF2) MANE Select | ENSP00000247668.2:n.*68G>C | |
| ENST00000247668.6:c.*68G>C (TRAF2) | ENSP00000247668.2:n.*68G>C | |
| ENST00000432842.6:c.*1038-31750G>C (RABL6) | ENSP00000414081.3:n.*1038-31750G>C | |
| NM_021138.3:c.*68G>C (TRAF2) | NP_066961.2:n.*68G>C | |
| XM_005266099.3:c.*68G>C (TRAF2) | XP_005266156.1:n.*68G>C | |
| XM_011518973.1:c.*68G>C (TRAF2) | XP_011517275.1:n.*68G>C | |
| XM_011518974.1:c.*68G>C (TRAF2) | XP_011517276.1:n.*68G>C | |
| XM_011518975.1:c.*68G>C (TRAF2) | XP_011517277.1:n.*68G>C | |
| XM_011518976.1:c.*68G>C (TRAF2) | XP_011517278.1:n.*68G>C | |
| XM_011518977.1:c.*68G>C (TRAF2) | XP_011517279.1:n.*68G>C | |
| XM_011518978.1:c.*68G>C (TRAF2) | XP_011517280.1:n.*68G>C | |
| XM_011518974.2:c.*68G>C (TRAF2) | XP_011517276.1:n.*68G>C | |
| XM_011518976.3:c.*68G>C (TRAF2) | XP_011517278.1:n.*68G>C | |
| XM_011518977.2:c.*68G>C (TRAF2) | XP_011517279.1:n.*68G>C | |
| NM_021138.4:c.*68G>C (TRAF2) MANE Select | NP_066961.2:n.*68G>C |