Linked Data
ClinVar Variation Id:
619727
dbSNP Id:
rs1568708275
MyVariant Identifiers:
chr19:g.1220675C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1220676C>T , CM000681.2:g.1220676C>T | GRCh38 |
| NC_000019.9:g.1220675C>T , CM000681.1:g.1220675C>T | GRCh37 |
| NC_000019.8:g.1171675C>T | NCBI36 |
| NG_007460.2:g.36270C>T , LRG_319:g.36270C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.693C>T | ENSP00000490268.2:p.Phe231= | |
| ENST00000585748.3:c.321C>T | ENSP00000477641.2:p.Phe107= | |
| ENST00000585851.2:c.519C>T | ENSP00000467912.2:p.Phe173= | |
| ENST00000326873.12:c.693C>T MANE Select | ENSP00000324856.6:p.Phe231= | |
| ENST00000652231.1:c.693C>T | ENSP00000498804.1:p.Phe231= | |
| ENST00000326873.11:c.693C>T | ENSP00000324856.6:p.Phe231= | |
| ENST00000586243.5:c.693C>T | ENSP00000467240.2:p.Phe231= | |
| ENST00000586358.5:n.591C>T | ||
| ENST00000589152.5:n.783C>T | ||
| ENST00000591133.2:n.664C>T | ||
| NM_000455.4:c.693C>T , LRG_319t1:c.693C>T | NP_000446.1:p.Phe231= | |
| XM_005259617.1:c.693C>T | XP_005259674.1:p.Phe231= | |
| XM_005259618.3:c.693C>T | XP_005259675.1:p.Phe231= | |
| XM_011528209.1:c.471C>T | XP_011526511.1:p.Phe157= | |
| XR_936204.1:n.1318C>T | ||
| XM_005259617.3:c.693C>T | XP_005259674.1:p.Phe231= | |
| XM_011528209.2:c.471C>T | XP_011526511.1:p.Phe157= | |
| XR_001753738.2:n.1318C>T | ||
| XR_001753739.1:n.1318C>T | ||
| XR_001753740.2:n.1318C>T | ||
| NM_000455.5:c.693C>T MANE Select | NP_000446.1:p.Phe231= |