Linked Data
ClinVar Variation Id:
439117
ClinVar RCV Id:
RCV000507294
dbSNP Id:
rs33933481
COSMIC:
COSM3817536
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173550G>T , CM000678.2:g.173550G>T | GRCh38 |
| NC_000016.9:g.223549G>T , CM000678.1:g.223549G>T | GRCh37 |
| NC_000016.8:g.163549G>T | NCBI36 |
| NG_000006.1:g.34413G>T | |
| NG_059186.1:g.1900G>T | |
| NG_059271.1:g.5704G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.379G>T MANE Select | ENSP00000251595.6:p.Asp127Tyr | |
| ENST00000251595.10:c.379G>T | ENSP00000251595.6:p.Asp127Tyr | |
| ENST00000397806.1:c.283G>T | ENSP00000380908.1:p.Asp95Tyr | |
| ENST00000482565.1:n.515G>T | ||
| NM_000517.4:c.379G>T | NP_000508.1:p.Asp127Tyr | |
| NM_000517.6:c.379G>T MANE Select | NP_000508.1:p.Asp127Tyr |