Linked Data
ClinVar Variation Id:
7001
dbSNP Id:
rs121909487
gnomAD v4:
9-126693243-C-T
PubMed:
PMID:9590287
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.126693243C>T , CM000671.2:g.126693243C>T | GRCh38 |
| NC_000009.11:g.129455522C>T , CM000671.1:g.129455522C>T | GRCh37 |
| NC_000009.10:g.128495343C>T | NCBI36 |
| NG_017039.1:g.83801C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355497.10:c.661C>T | ENSP00000347684.5:p.Arg221Ter | |
| ENST00000373474.9:c.661C>T MANE Select | ENSP00000362573.3:p.Arg221Ter | |
| ENST00000526117.6:c.661C>T | ENSP00000436930.1:p.Arg221Ter | |
| ENST00000355497.9:c.661C>T | ENSP00000347684.5:p.Arg221Ter | |
| ENST00000373474.8:c.661C>T | ENSP00000362573.3:p.Arg221Ter | |
| ENST00000526117.5:c.661C>T | ENSP00000436930.1:p.Arg221Ter | |
| ENST00000561065.1:c.592C>T | ENSP00000453580.1:p.Arg198Ter | |
| NM_001174146.1:c.661C>T | NP_001167617.1:p.Arg221Ter | |
| NM_001174147.1:c.661C>T | NP_001167618.1:p.Arg221Ter | |
| NM_002316.3:c.661C>T | NP_002307.2:p.Arg221Ter | |
| NM_001174146.2:c.661C>T | NP_001167617.1:p.Arg221Ter | |
| NM_001174147.2:c.661C>T MANE Select | NP_001167618.1:p.Arg221Ter | |
| NM_002316.4:c.661C>T | NP_002307.2:p.Arg221Ter |