Linked Data
ClinVar Variation Id:
2604874
ClinVar RCV Id:
RCV003359539
dbSNP Id:
rs564798632
gnomAD v2:
12-5154217-G-T
gnomAD v4:
12-5045051-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5045051G>T , CM000674.2:g.5045051G>T | GRCh38 |
| NC_000012.11:g.5154217G>T , CM000674.1:g.5154217G>T | GRCh37 |
| NC_000012.10:g.5024478G>T | NCBI36 |
| NG_012198.1:g.6133G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.904G>T MANE Select | ENSP00000252321.3:p.Gly302Trp | |
| ENST00000252321.4:c.904G>T | ENSP00000252321.3:p.Gly302Trp | |
| NM_002234.3:c.904G>T | NP_002225.2:p.Gly302Trp | |
| NM_002234.4:c.904G>T MANE Select | NP_002225.2:p.Gly302Trp |