Linked Data
ClinVar Variation Id:
101150
ClinVar RCV Id:
RCV000087387
dbSNP Id:
rs587779458
gnomAD v4:
2-188999331-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188999331G>T , CM000664.2:g.188999331G>T | GRCh38 |
| NC_000002.11:g.189864057G>T , CM000664.1:g.189864057G>T | GRCh37 |
| NC_000002.10:g.189572302G>T | NCBI36 |
| NG_007404.1:g.29959G>T , LRG_3:g.29959G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.1970G>T | ENSP00000415346.2:p.Gly657Val | |
| ENST00000304636.9:c.2069G>T MANE Select | ENSP00000304408.4:p.Gly690Val | |
| ENST00000304636.7:c.2069G>T | ENSP00000304408.3:p.Gly690Val | |
| ENST00000317840.9:c.2069G>T | ENSP00000315243.6:p.Gly690Val | |
| NM_000090.3:c.2069G>T , LRG_3t1:c.2069G>T | NP_000081.1:p.Gly690Val | |
| NM_000090.4:c.2069G>T MANE Select | NP_000081.2:p.Gly690Val |