Linked Data
ClinVar Variation Id:
204134
ClinVar RCV Id:
RCV000186340
dbSNP Id:
rs180177288
gnomAD v4:
2-240877543-G-T
PubMed:
PMID:19479957
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240877543G>T , CM000664.2:g.240877543G>T | GRCh38 |
| NC_000002.11:g.241816960G>T , CM000664.1:g.241816960G>T | GRCh37 |
| NC_000002.10:g.241465633G>T | NCBI36 |
| NG_008005.1:g.13799G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.853G>T MANE Select | ENSP00000302620.3:p.Glu285Ter | |
| ENST00000307503.3:c.853G>T | ENSP00000302620.3:p.Glu285Ter | |
| ENST00000470255.1:n.631G>T | ||
| NM_000030.2:c.853G>T | NP_000021.1:p.Glu285Ter | |
| NM_000030.3:c.853G>T MANE Select | NP_000021.1:p.Glu285Ter |