Linked Data
ClinVar Variation Id:
229269
dbSNP Id:
rs147474792
ExAC:
15:38641627 C / T
gnomAD v2:
15-38641627-C-T
gnomAD v3:
15-38349426-C-T
gnomAD v4:
15-38349426-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38349426C>T , CM000677.2:g.38349426C>T | GRCh38 |
| NC_000015.9:g.38641627C>T , CM000677.1:g.38641627C>T | GRCh37 |
| NC_000015.8:g.36428919C>T | NCBI36 |
| NG_008980.1:g.101576C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.587C>T MANE Select | ENSP00000299084.4:p.Thr196Ile | |
| ENST00000299084.8:c.587C>T | ENSP00000299084.4:p.Thr196Ile | |
| NM_152594.2:c.587C>T | NP_689807.1:p.Thr196Ile | |
| XM_005254202.2:c.623C>T | XP_005254259.1:p.Thr208Ile | |
| XM_005254203.3:c.365C>T | XP_005254260.1:p.Thr122Ile | |
| XM_011521288.1:c.524C>T | XP_011519590.1:p.Thr175Ile | |
| XM_011521289.1:c.524C>T | XP_011519591.1:p.Thr175Ile | |
| XM_011521290.1:c.524C>T | XP_011519592.1:p.Thr175Ile | |
| XM_005254202.3:c.623C>T | XP_005254259.1:p.Thr208Ile | |
| XM_011521289.3:c.524C>T | XP_011519591.1:p.Thr175Ile | |
| NM_152594.3:c.587C>T MANE Select | NP_689807.1:p.Thr196Ile |