Linked Data
ClinVar Variation Id:
200045
dbSNP Id:
rs794728223
gnomAD v4:
15-48470646-C-T
COSMIC:
COSM4055309
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48470646C>T , CM000677.2:g.48470646C>T | GRCh38 |
| NC_000015.9:g.48762843C>T , CM000677.1:g.48762843C>T | GRCh37 |
| NC_000015.8:g.46550135C>T | NCBI36 |
| NG_008805.2:g.180143G>A , LRG_778:g.180143G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.4447G>A | ENSP00000453958.2:p.Gly1483Arg | |
| ENST00000674301.2:c.4447G>A | ENSP00000501333.2:p.Gly1483Arg | |
| ENST00000683268.1:n.414G>A | ||
| ENST00000684448.1:n.3121G>A | ||
| ENST00000316623.10:c.4447G>A MANE Select | ENSP00000325527.5:p.Gly1483Arg | |
| ENST00000316623.9:c.4447G>A | ENSP00000325527.5:p.Gly1483Arg | |
| ENST00000537463.6:c.*210G>A | ENSP00000440294.2:n.*210G>A | |
| NM_000138.4:c.4447G>A , LRG_778t1:c.4447G>A | NP_000129.3:p.Gly1483Arg | |
| NM_000138.5:c.4447G>A MANE Select | NP_000129.3:p.Gly1483Arg |