Linked Data
ClinVar Variation Id:
621
dbSNP Id:
rs118203923
ExAC:
12:103246704 G / A
gnomAD v2:
12-103246704-G-A
gnomAD v4:
12-102852926-G-A
ERepo:
CA229721/MONDO:0009861/006
PubMed:
PMID:1363838
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102852926G>A , CM000674.2:g.102852926G>A | GRCh38 |
| NC_000012.11:g.103246704G>A , CM000674.1:g.103246704G>A | GRCh37 |
| NC_000012.10:g.101770834G>A | NCBI36 |
| NG_008690.1:g.69677C>T | |
| NG_008690.2:g.110485C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.731C>T MANE Select | ENSP00000448059.1:p.Pro244Leu | |
| ENST00000307000.7:c.716C>T | ENSP00000303500.2:p.Pro239Leu | |
| ENST00000549247.6:n.490C>T | ||
| ENST00000553106.5:c.731C>T | ENSP00000448059.1:p.Pro244Leu | |
| NM_000277.1:c.731C>T | NP_000268.1:p.Pro244Leu | |
| XM_011538422.1:c.731C>T | XP_011536724.1:p.Pro244Leu | |
| NM_000277.2:c.731C>T | NP_000268.1:p.Pro244Leu | |
| NM_001354304.1:c.731C>T | NP_001341233.1:p.Pro244Leu | |
| NM_000277.3:c.731C>T MANE Select | NP_000268.1:p.Pro244Leu | |
| NM_001354304.2:c.731C>T | NP_001341233.1:p.Pro244Leu |