Linked Data
ClinVar Variation Id:
240998
dbSNP Id:
rs78102263
ExAC:
2:73678054 G / T
gnomAD v2:
2-73678054-G-T
gnomAD v3:
2-73450927-G-T
gnomAD v4:
2-73450927-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73450927G>T , CM000664.2:g.73450927G>T | GRCh38 |
| NC_000002.11:g.73678054G>T , CM000664.1:g.73678054G>T | GRCh37 |
| NC_000002.10:g.73531562G>T | NCBI36 |
| NG_011690.1:g.70175G>T , LRG_741:g.70175G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682565.1:c.4019G>T | ENSP00000507671.1:p.Gly1340Val | |
| ENST00000682801.1:c.4019G>T | ENSP00000507862.1:p.Gly1340Val | |
| ENST00000682859.1:c.4019G>T | ENSP00000508222.1:p.Gly1340Val | |
| ENST00000683791.1:c.685+18636G>T | ||
| ENST00000684460.1:c.1471G>T | ||
| ENST00000684548.1:c.4019G>T | ENSP00000507421.1:p.Gly1340Val | |
| ENST00000684656.1:c.1471G>T | ||
| ENST00000613296.6:c.4400G>T MANE Select | ENSP00000482968.1:p.Gly1467Val | |
| ENST00000484298.5:c.4274G>T | ENSP00000478155.1:p.Gly1425Val | |
| ENST00000613296.4:c.4400G>T | ENSP00000482968.1:p.Gly1467Val | |
| ENST00000614410.4:c.4400G>T | ENSP00000479094.1:p.Gly1467Val | |
| NM_015120.4:c.4403G>T , LRG_741t1:c.4403G>T | NP_055935.4:p.Gly1468Val | |
| NM_001378454.1:c.4400G>T MANE Select | NP_001365383.1:p.Gly1467Val |