Linked Data
ClinVar Variation Id:
528053
ClinVar RCV Id:
RCV000633133
dbSNP Id:
rs139767471
ExAC:
9:130587628 G / A
gnomAD v2:
9-130587628-G-A
gnomAD v3:
9-127825349-G-A
gnomAD v4:
9-127825349-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127825349G>A , CM000671.2:g.127825349G>A | GRCh38 |
| NC_000009.11:g.130587628G>A , CM000671.1:g.130587628G>A | GRCh37 |
| NC_000009.10:g.129627449G>A | NCBI36 |
| NG_009551.1:g.34420C>T , LRG_589:g.34420C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480266.6:c.152C>T | ENSP00000479015.1:p.Thr51Met | |
| ENST00000373203.9:c.698C>T MANE Select | ENSP00000362299.4:p.Thr233Met | |
| ENST00000344849.4:c.698C>T | ENSP00000341917.3:p.Thr233Met | |
| ENST00000373203.8:c.698C>T | ENSP00000362299.4:p.Thr233Met | |
| ENST00000480266.5:c.152C>T | ENSP00000479015.1:p.Thr51Met | |
| NM_000118.3:c.698C>T , LRG_589t1:c.698C>T | NP_000109.1:p.Thr233Met | |
| NM_001114753.2:c.698C>T , LRG_589t2:c.698C>T | NP_001108225.1:p.Thr233Met | |
| NM_001278138.1:c.152C>T | NP_001265067.1:p.Thr51Met | |
| NM_001114753.3:c.698C>T MANE Select | NP_001108225.1:p.Thr233Met | |
| NM_001278138.2:c.152C>T | NP_001265067.1:p.Thr51Met |