Linked Data
ClinVar Variation Id:
2433674
ClinVar RCV Id:
RCV003131563
dbSNP Id:
rs2143251369
COSMIC:
COSM6474922
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.72123686G>T , CM000679.2:g.72123686G>T | GRCh38 |
| NC_000017.10:g.70119827G>T , CM000679.1:g.70119827G>T | GRCh37 |
| NC_000017.9:g.67631422G>T | NCBI36 |
| NG_012490.1:g.7667G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245479.3:c.829G>T MANE Select | ENSP00000245479.2:p.Glu277Ter | |
| ENST00000245479.2:c.829G>T | ENSP00000245479.2:p.Glu277Ter | |
| NM_000346.3:c.829G>T | NP_000337.1:p.Glu277Ter | |
| NM_000346.4:c.829G>T MANE Select | NP_000337.1:p.Glu277Ter |