Linked Data
dbSNP Id:
rs764019661
ExAC:
16:81391496 T / A
gnomAD v2:
16-81391496-T-A
gnomAD v3:
16-81357891-T-A
gnomAD v4:
16-81357891-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81357891T>A , CM000678.2:g.81357891T>A | GRCh38 |
| NC_000016.9:g.81391496T>A , CM000678.1:g.81391496T>A | GRCh37 |
| NC_000016.8:g.79948997T>A | NCBI36 |
| NG_009007.1:g.47926T>A , LRG_242:g.47926T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*641T>A | ENSP00000498114.1:n.*641T>A | |
| ENST00000648994.2:c.933T>A MANE Select | ENSP00000497351.1:p.Pro311= | |
| ENST00000650388.1:c.467T>A | ENSP00000498081.1:n.467T>A | |
| ENST00000568107.2:c.933T>A | ENSP00000476795.1:p.Pro311= | |
| NM_022041.3:c.933T>A , LRG_242t1:c.933T>A | NP_071324.1:p.Pro311= | |
| XM_017023734.1:c.294T>A | XP_016879223.1:p.Pro98= | |
| NM_001377486.1:c.294T>A | NP_001364415.1:p.Pro98= | |
| NM_022041.4:c.933T>A MANE Select | NP_071324.1:p.Pro311= |