Linked Data
dbSNP Id:
rs957070137
gnomAD v2:
16-50766878-A-T
gnomAD v3:
16-50732967-A-T
gnomAD v4:
16-50732967-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.50732967A>T , CM000678.2:g.50732967A>T | GRCh38 |
| NC_000016.9:g.50766878A>T , CM000678.1:g.50766878A>T | GRCh37 |
| NC_000016.8:g.49324379A>T | NCBI36 |
| NG_007508.1:g.40829A>T , LRG_177:g.40829A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641284.2:c.*1304A>T | ENSP00000493088.1:n.*1304A>T | |
| ENST00000646677.2:c.*1955A>T | ENSP00000496533.1:n.*1955A>T | |
| ENST00000697428.1:n.3668A>T | ||
| ENST00000641284.1:c.*1304A>T | ENSP00000493088.1:n.*1304A>T | |
| ENST00000646677.1:c.*1955A>T | ENSP00000496533.1:n.*1955A>T | |
| ENST00000647318.2:c.*1148A>T MANE Select | ENSP00000495993.1:n.*1148A>T | |
| ENST00000300589.6:c.*1148A>T | ENSP00000300589.2:n.*1148A>T | |
| NM_001293557.1:c.*1148A>T | NP_001280486.1:n.*1148A>T | |
| NM_022162.2:c.*1148A>T | NP_071445.1:n.*1148A>T | |
| XM_005256084.2:c.*1148A>T | XP_005256141.1:n.*1148A>T | |
| XM_006721242.2:c.*1148A>T | XP_006721305.1:n.*1148A>T | |
| XM_011523257.1:c.*1148A>T | XP_011521559.1:n.*1148A>T | |
| XM_011523258.1:c.*1148A>T | XP_011521560.1:n.*1148A>T | |
| XM_011523259.1:c.*1148A>T | XP_011521561.1:n.*1148A>T | |
| XM_005256084.4:c.*1148A>T | XP_005256141.1:n.*1148A>T | |
| XM_006721242.4:c.*1148A>T | XP_006721305.1:n.*1148A>T | |
| XM_011523259.2:c.*1148A>T | XP_011521561.1:n.*1148A>T | |
| XM_017023535.1:c.*1148A>T | XP_016879024.1:n.*1148A>T | |
| XM_017023536.1:c.*1148A>T | XP_016879025.1:n.*1148A>T | |
| XM_017023537.1:c.*1148A>T | XP_016879026.1:n.*1148A>T | |
| XM_017023538.1:c.*1148A>T | XP_016879027.1:n.*1148A>T | |
| NM_001293557.2:c.*1148A>T | NP_001280486.1:n.*1148A>T | |
| NM_001370466.1:c.*1148A>T MANE Select | NP_001357395.1:n.*1148A>T | |
| NM_022162.3:c.*1148A>T | NP_071445.1:n.*1148A>T | |
| NR_163434.1:n.4402A>T |