Linked Data
dbSNP Id:
rs778782236
ExAC:
6:139694417 A / C
gnomAD v2:
6-139694417-A-C
gnomAD v4:
6-139373280-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.139373280A>C , CM000668.2:g.139373280A>C | GRCh38 |
| NC_000006.11:g.139694417A>C , CM000668.1:g.139694417A>C | GRCh37 |
| NC_000006.10:g.139736110A>C | NCBI36 |
| NG_016169.1:g.6369T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367651.4:c.665T>G MANE Select | ENSP00000356623.2:p.Phe222Cys | |
| ENST00000367651.3:c.665T>G | ENSP00000356623.2:p.Phe222Cys | |
| ENST00000536159.2:c.665T>G | ENSP00000442831.1:p.Phe222Cys | |
| ENST00000537332.2:c.680T>G | ENSP00000444198.2:p.Phe227Cys | |
| ENST00000618718.1:c.494T>G | ENSP00000479918.1:p.Phe165Cys | |
| NM_001168388.2:c.665T>G | NP_001161860.1:p.Phe222Cys | |
| NM_001168389.2:c.680T>G | NP_001161861.2:p.Phe227Cys | |
| NM_006079.4:c.665T>G | NP_006070.2:p.Phe222Cys | |
| NM_006079.5:c.665T>G MANE Select | NP_006070.2:p.Phe222Cys | |
| NM_001168388.3:c.665T>G | NP_001161860.1:p.Phe222Cys | |
| NM_001168389.3:c.680T>G | NP_001161861.2:p.Phe227Cys |