Linked Data
ClinVar Variation Id:
2988212
ClinVar RCV Id:
RCV003844395
dbSNP Id:
rs888211462
gnomAD v2:
19-30199314-T-C
gnomAD v3:
19-29708407-T-C
gnomAD v4:
19-29708407-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.29708407T>C , CM000681.2:g.29708407T>C | GRCh38 |
| NC_000019.9:g.30199314T>C , CM000681.1:g.30199314T>C | GRCh37 |
| NC_000019.8:g.34891154T>C | NCBI36 |
| NG_031970.1:g.12383A>G | |
| NG_031970.2:g.12383A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614091.5:c.7A>G | ENSP00000482097.2:p.Ile3Val | |
| ENST00000623113.3:c.7A>G | ENSP00000485413.2:p.Ile3Val | |
| ENST00000323670.14:c.7A>G MANE Select | ENSP00000313332.9:p.Ile3Val | |
| ENST00000323670.13:c.7A>G | ENSP00000313332.8:p.Ile3Val | |
| ENST00000342680.5:c.7A>G | ENSP00000345497.5:p.Ile3Val | |
| ENST00000392275.1:n.552-5430A>G | ||
| ENST00000392276.1:c.-32-5430A>G | ENSP00000376102.1:n.-32-5430A>G | |
| ENST00000392278.2:c.40A>G | ENSP00000376103.2:p.Ile14Val | |
| ENST00000591243.1:c.7A>G | ENSP00000467516.1:p.Ile3Val | |
| ENST00000592153.5:c.7A>G | ENSP00000467117.1:p.Ile3Val | |
| ENST00000614091.4:c.7A>G | ENSP00000482097.1:p.Ile3Val | |
| ENST00000623113.1:c.-32-5430A>G | ENSP00000485413.1:n.-32-5430A>G | |
| NM_001031726.3:c.40A>G | NP_001026896.2:p.Ile14Val | |
| NM_001256046.1:c.7A>G | NP_001242975.1:p.Ile3Val | |
| NM_001256047.1:c.7A>G | NP_001242976.1:p.Ile3Val | |
| NM_001282929.1:c.-32-5430A>G | NP_001269858.1:n.-32-5430A>G | |
| NM_001282930.1:c.-32-5430A>G | NP_001269859.1:n.-32-5430A>G | |
| NM_001282931.1:c.-307A>G | NP_001269860.1:n.-307A>G | |
| NM_031448.4:c.7A>G | NP_113636.2:p.Ile3Val | |
| XM_024451734.1:c.169A>G | XP_024307502.1:p.Ile57Val | |
| XM_024451735.1:c.7A>G | XP_024307503.1:p.Ile3Val | |
| XM_024451736.1:c.7A>G | XP_024307504.1:p.Ile3Val | |
| XM_024451737.1:c.7A>G | XP_024307505.1:p.Ile3Val | |
| XM_024451738.1:c.7A>G | XP_024307506.1:p.Ile3Val | |
| NM_001256046.2:c.7A>G | NP_001242975.1:p.Ile3Val | |
| NM_001282930.2:c.-32-5430A>G | NP_001269859.1:n.-32-5430A>G | |
| NM_001282931.2:c.-307A>G | NP_001269860.1:n.-307A>G | |
| NM_031448.6:c.7A>G MANE Select | NP_113636.2:p.Ile3Val | |
| NM_001031726.4:c.7A>G | NP_001026896.3:p.Ile3Val | |
| NM_001256046.3:c.7A>G | NP_001242975.1:p.Ile3Val | |
| NM_001256047.2:c.7A>G | NP_001242976.1:p.Ile3Val | |
| NM_001282930.3:c.-32-5430A>G | NP_001269859.1:n.-32-5430A>G | |
| NM_001282931.3:c.-307A>G | NP_001269860.1:n.-307A>G |