Linked Data
ClinVar Variation Id:
421771
ClinVar RCV Id:
RCV000486276
dbSNP Id:
rs768424025
ExAC:
8:27320842 C / G
gnomAD v2:
8-27320842-C-G
gnomAD v4:
8-27463325-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.27463325C>G , CM000670.2:g.27463325C>G | GRCh38 |
| NC_000008.10:g.27320842C>G , CM000670.1:g.27320842C>G | GRCh37 |
| NC_000008.9:g.27376759C>G | NCBI36 |
| NG_015827.1:g.20972G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000407991.3:c.1118G>C MANE Select | ENSP00000385026.1:p.Cys373Ser | |
| ENST00000240132.7:c.1073G>C | ENSP00000240132.2:p.Cys358Ser | |
| ENST00000407991.2:c.1118G>C | ENSP00000385026.1:p.Cys373Ser | |
| ENST00000520600.1:n.290-1571G>C | ||
| ENST00000520933.7:c.1052G>C | ENSP00000429616.2:p.Cys351Ser | |
| ENST00000523695.5:c.*520G>C | ENSP00000430612.1:n.*520G>C | |
| NM_000742.3:c.1118G>C | NP_000733.2:p.Cys373Ser | |
| NM_001282455.1:c.1073G>C | NP_001269384.1:p.Cys358Ser | |
| XM_005273397.1:c.641G>C | XP_005273454.1:p.Cys214Ser | |
| XM_006716282.1:c.1118G>C | XP_006716345.1:p.Cys373Ser | |
| XM_011544388.1:c.1118G>C | XP_011542690.1:p.Cys373Ser | |
| XM_011544389.1:c.524G>C | XP_011542691.1:p.Cys175Ser | |
| NM_001347705.1:c.641G>C | NP_001334634.1:p.Cys214Ser | |
| NM_001347706.1:c.641G>C | NP_001334635.1:p.Cys214Ser | |
| NM_001347707.1:c.524G>C | NP_001334636.1:p.Cys175Ser | |
| NM_001347708.1:c.524G>C | NP_001334637.1:p.Cys175Ser | |
| XM_011544389.2:c.524G>C | XP_011542691.1:p.Cys175Ser | |
| NM_000742.4:c.1118G>C MANE Select | NP_000733.2:p.Cys373Ser | |
| NM_001282455.2:c.1073G>C | NP_001269384.1:p.Cys358Ser | |
| NM_001347705.2:c.641G>C | NP_001334634.1:p.Cys214Ser | |
| NM_001347706.2:c.641G>C | NP_001334635.1:p.Cys214Ser | |
| NM_001347707.2:c.524G>C | NP_001334636.1:p.Cys175Ser | |
| NM_001347708.2:c.524G>C | NP_001334637.1:p.Cys175Ser |