Linked Data
ClinVar Variation Id:
2758623
ClinVar RCV Id:
RCV003569791
MyVariant Identifiers:
chr19:g.18900083G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18789274G>C , CM000681.2:g.18789274G>C | GRCh38 |
| NC_000019.9:g.18900083G>C , CM000681.1:g.18900083G>C | GRCh37 |
| NC_000019.8:g.18761083G>C | NCBI36 |
| NG_007070.1:g.7032C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.414C>G MANE Select | ENSP00000222271.2:p.Pro138= | |
| ENST00000222271.6:c.414C>G | ENSP00000222271.2:p.Pro138= | |
| ENST00000425807.1:c.391-382C>G | ENSP00000403792.1:n.391-382C>G | |
| ENST00000542601.6:c.315C>G | ENSP00000439156.2:p.Pro105= | |
| NM_000095.2:c.414C>G | NP_000086.2:p.Pro138= | |
| NM_000095.3:c.414C>G MANE Select | NP_000086.2:p.Pro138= |