Linked Data
ClinVar Variation Id:
204131
ClinVar RCV Id:
RCV000186337
dbSNP Id:
rs180177279
gnomAD v4:
2-240876002-C-T
PubMed:
PMID:15365967
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240876002C>T , CM000664.2:g.240876002C>T | GRCh38 |
| NC_000002.11:g.241815419C>T , CM000664.1:g.241815419C>T | GRCh37 |
| NC_000002.10:g.241464092C>T | NCBI36 |
| NG_008005.1:g.12258C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.844C>T MANE Select | ENSP00000302620.3:p.Gln282Ter | |
| ENST00000307503.3:c.844C>T | ENSP00000302620.3:p.Gln282Ter | |
| ENST00000476698.1:n.496C>T | ||
| NM_000030.2:c.844C>T | NP_000021.1:p.Gln282Ter | |
| NM_000030.3:c.844C>T MANE Select | NP_000021.1:p.Gln282Ter |