Linked Data
dbSNP Id:
rs780257155
ExAC:
6:139694228 A / T
gnomAD v2:
6-139694228-A-T
gnomAD v4:
6-139373091-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.139373091A>T , CM000668.2:g.139373091A>T | GRCh38 |
| NC_000006.11:g.139694228A>T , CM000668.1:g.139694228A>T | GRCh37 |
| NC_000006.10:g.139735921A>T | NCBI36 |
| NG_016169.1:g.6558T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367651.4:c.*41T>A MANE Select | ENSP00000356623.2:n.*41T>A | |
| ENST00000367651.3:c.*41T>A | ENSP00000356623.2:n.*41T>A | |
| ENST00000536159.2:c.*41T>A | ENSP00000442831.1:n.*41T>A | |
| ENST00000537332.2:c.*41T>A | ENSP00000444198.2:n.*41T>A | |
| ENST00000618718.1:c.*41T>A | ENSP00000479918.1:n.*41T>A | |
| NM_001168388.2:c.*41T>A | NP_001161860.1:n.*41T>A | |
| NM_001168389.2:c.*41T>A | NP_001161861.2:n.*41T>A | |
| NM_006079.4:c.*41T>A | NP_006070.2:n.*41T>A | |
| NM_006079.5:c.*41T>A MANE Select | NP_006070.2:n.*41T>A | |
| NM_001168388.3:c.*41T>A | NP_001161860.1:n.*41T>A | |
| NM_001168389.3:c.*41T>A | NP_001161861.2:n.*41T>A |