Linked Data
ClinVar Variation Id:
594046
dbSNP Id:
rs184769421
ExAC:
16:8900223 C / T
gnomAD v2:
16-8900223-C-T
gnomAD v3:
16-8806366-C-T
gnomAD v4:
16-8806366-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.8806366C>T , CM000678.2:g.8806366C>T | GRCh38 |
| NC_000016.9:g.8900223C>T , CM000678.1:g.8900223C>T | GRCh37 |
| NC_000016.8:g.8807724C>T | NCBI36 |
| NG_009209.1:g.13554C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682008.1:c.306C>T | ENSP00000507849.1:p.Tyr102= | |
| ENST00000682393.1:c.178+4456C>T | ENSP00000506774.1:n.178+4456C>T | |
| ENST00000683094.1:c.*28C>T | ENSP00000508230.1:n.*28C>T | |
| ENST00000683274.1:c.306C>T | ENSP00000507262.1:p.Tyr102= | |
| ENST00000683435.1:c.*302C>T | ENSP00000508092.1:n.*302C>T | |
| ENST00000268261.9:c.306C>T MANE Select | ENSP00000268261.4:p.Tyr102= | |
| ENST00000268261.8:c.306C>T | ENSP00000268261.4:p.Tyr102= | |
| ENST00000562318.5:c.*28C>T | ENSP00000454395.1:n.*28C>T | |
| ENST00000562448.1:n.270C>T | ||
| ENST00000564030.5:n.368C>T | ||
| ENST00000564069.1:c.277C>T | ||
| ENST00000565221.5:c.178+4456C>T | ENSP00000457932.1:n.178+4456C>T | |
| ENST00000565896.5:c.*145+3977C>T | ENSP00000456024.1:n.*145+3977C>T | |
| ENST00000566540.5:c.*28C>T | ENSP00000454284.1:n.*28C>T | |
| ENST00000566604.5:c.306C>T | ENSP00000456774.1:p.Tyr102= | |
| ENST00000566983.5:c.225C>T | ENSP00000457956.1:p.Tyr75= | |
| ENST00000568602.5:c.*159C>T | ENSP00000455066.1:n.*159C>T | |
| ENST00000569958.5:c.178+4456C>T | ENSP00000456302.1:n.178+4456C>T | |
| ENST00000570076.5:c.178+4456C>T | ENSP00000456961.1:n.178+4456C>T | |
| ENST00000570134.5:c.*28C>T | ENSP00000456275.1:n.*28C>T | |
| NM_000303.2:c.306C>T | NP_000294.1:p.Tyr102= | |
| XM_005255372.3:c.306C>T | XP_005255429.1:p.Tyr102= | |
| XM_005255373.3:c.57C>T | XP_005255430.1:p.Tyr19= | |
| XM_005255374.3:c.57C>T | XP_005255431.1:p.Tyr19= | |
| XM_011522538.1:c.306C>T | XP_011520840.1:p.Tyr102= | |
| XM_011522539.1:c.-29+4456C>T | XP_011520841.1:n.-29+4456C>T | |
| XM_005255374.4:c.57C>T | XP_005255431.1:p.Tyr19= | |
| NM_000303.3:c.306C>T MANE Select | NP_000294.1:p.Tyr102= |