Linked Data
ClinVar Variation Id:
619167
ClinVar RCV Id:
RCV000758135
dbSNP Id:
rs749613899
ExAC:
12:103234277 T / C
gnomAD v2:
12-103234277-T-C
gnomAD v3:
12-102840499-T-C
gnomAD v4:
12-102840499-T-C
ERepo:
CA6748709/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102840499T>C , CM000674.2:g.102840499T>C | GRCh38 |
| NC_000012.11:g.103234277T>C , CM000674.1:g.103234277T>C | GRCh37 |
| NC_000012.10:g.101758407T>C | NCBI36 |
| NG_008690.1:g.82104A>G | |
| NG_008690.2:g.122912A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.1216A>G MANE Select | ENSP00000448059.1:p.Ile406Val | |
| ENST00000307000.7:c.1201A>G | ENSP00000303500.2:p.Ile401Val | |
| ENST00000551114.2:n.878A>G | ||
| ENST00000553106.5:c.1216A>G | ENSP00000448059.1:p.Ile406Val | |
| ENST00000635477.1:c.320A>G | ||
| ENST00000635528.1:n.731A>G | ||
| NM_000277.1:c.1216A>G | NP_000268.1:p.Ile406Val | |
| XM_011538422.1:c.1159A>G | XP_011536724.1:p.Ile387Val | |
| NM_000277.2:c.1216A>G | NP_000268.1:p.Ile406Val | |
| NM_001354304.1:c.1216A>G | NP_001341233.1:p.Ile406Val | |
| NM_000277.3:c.1216A>G MANE Select | NP_000268.1:p.Ile406Val | |
| NM_001354304.2:c.1216A>G | NP_001341233.1:p.Ile406Val |