Linked Data
ClinVar Variation Id:
408426
ClinVar RCV Id:
RCV000615791
dbSNP Id:
rs201129153
ExAC:
1:218614599 C / T
gnomAD v2:
1-218614599-C-T
gnomAD v3:
1-218441257-C-T
gnomAD v4:
1-218441257-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.218441257C>T , CM000663.2:g.218441257C>T | GRCh38 |
| NC_000001.10:g.218614599C>T , CM000663.1:g.218614599C>T | GRCh37 |
| NC_000001.9:g.216681222C>T | NCBI36 |
| NG_027721.1:g.100924C>T | |
| NG_027721.2:g.100924C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000366930.9:c.1140C>T MANE Select | ENSP00000355897.4:p.Cys380= | |
| ENST00000366929.4:c.1224C>T | ENSP00000355896.4:p.Cys408= | |
| ENST00000366930.8:c.1140C>T | ENSP00000355897.4:p.Cys380= | |
| ENST00000479322.1:n.624C>T | ||
| NM_001135599.2:c.1224C>T | NP_001129071.1:p.Cys408= | |
| NM_003238.3:c.1140C>T | NP_003229.1:p.Cys380= | |
| NM_001135599.3:c.1224C>T | NP_001129071.1:p.Cys408= | |
| NM_003238.4:c.1140C>T | NP_003229.1:p.Cys380= | |
| NR_138148.1:n.2443C>T | ||
| NR_138149.1:n.2527C>T | ||
| NM_003238.5:c.1140C>T | NP_003229.1:p.Cys380= | |
| NM_003238.6:c.1140C>T MANE Select | NP_003229.1:p.Cys380= | |
| NM_001135599.4:c.1224C>T | NP_001129071.1:p.Cys408= | |
| NR_138148.2:n.2391C>T | ||
| NR_138149.2:n.2475C>T |