Linked Data
ClinVar Variation Id:
430567
dbSNP Id:
rs1131692030
gnomAD v2:
19-13007024-C-T
gnomAD v3:
19-12896210-C-T
gnomAD v4:
19-12896210-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12896210C>T , CM000681.2:g.12896210C>T | GRCh38 |
| NC_000019.9:g.13007024C>T , CM000681.1:g.13007024C>T | GRCh37 |
| NC_000019.8:g.12868024C>T | NCBI36 |
| NG_009292.1:g.10051C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222214.10:c.641C>T MANE Select | ENSP00000222214.4:p.Thr214Met | |
| ENST00000222214.9:c.641C>T | ENSP00000222214.4:p.Thr214Met | |
| ENST00000421816.6:n.619C>T | ||
| ENST00000585420.5:n.1001-30C>T | ||
| ENST00000590530.5:c.*81C>T | ENSP00000468452.1:n.*81C>T | |
| ENST00000591043.1:n.677C>T | ||
| ENST00000591470.5:c.641C>T | ENSP00000466845.1:p.Thr214Met | |
| NM_000159.3:c.641C>T | NP_000150.1:p.Thr214Met | |
| NM_013976.3:c.641C>T | NP_039663.1:p.Thr214Met | |
| NR_102316.1:n.804C>T | ||
| NR_102317.1:n.1052-30C>T | ||
| XM_006722721.2:c.641C>T | XP_006722784.1:p.Thr214Met | |
| XM_011527899.1:c.641C>T | XP_011526201.1:p.Thr214Met | |
| XM_011527900.1:c.641C>T | XP_011526202.1:p.Thr214Met | |
| XM_011527899.2:c.641C>T | XP_011526201.1:p.Thr214Met | |
| XM_011527900.2:c.641C>T | XP_011526202.1:p.Thr214Met | |
| XM_017026580.1:c.641C>T | XP_016882069.1:p.Thr214Met | |
| NM_000159.4:c.641C>T MANE Select | NP_000150.1:p.Thr214Met | |
| NM_013976.4:c.641C>T | NP_039663.1:p.Thr214Met | |
| NM_013976.5:c.641C>T | NP_039663.1:p.Thr214Met |