Linked Data
ClinVar Variation Id:
10112
ClinVar RCV Id:
RCV000010824
dbSNP Id:
rs137852361
PubMed:
PMID:2105906
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154928677G>A , CM000685.2:g.154928677G>A | GRCh38 |
| NC_000023.10:g.154156952G>A , CM000685.1:g.154156952G>A | GRCh37 |
| NC_000023.9:g.153810146G>A | NCBI36 |
| NG_011403.1:g.99047C>T | |
| NG_011403.2:g.99047C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.5113C>T MANE Select | ENSP00000353393.4:p.Gln1705Ter | |
| ENST00000360256.8:c.5113C>T | ENSP00000353393.4:p.Gln1705Ter | |
| NM_000132.3:c.5113C>T | NP_000123.1:p.Gln1705Ter | |
| XM_011531126.1:c.5008C>T | XP_011529428.1:p.Gln1670Ter | |
| NM_000132.4:c.5113C>T MANE Select | NP_000123.1:p.Gln1705Ter |