Linked Data
ClinVar Variation Id:
1782767
ClinVar RCV Id:
RCV002410800
dbSNP Id:
rs1043732204
MyVariant Identifiers:
chr16:g.15844127G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.15750270G>C , CM000678.2:g.15750270G>C | GRCh38 |
| NC_000016.9:g.15844127G>C , CM000678.1:g.15844127G>C | GRCh37 |
| NC_000016.8:g.15751628G>C | NCBI36 |
| NG_009299.1:g.111761C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300036.6:c.1926C>G MANE Select | ENSP00000300036.5:p.Ala642= | |
| ENST00000452625.7:c.1947C>G MANE Plus Clinical | ENSP00000407821.2:p.Ala649= | |
| ENST00000576790.7:c.1926C>G | ENSP00000458731.1:p.Ala642= | |
| ENST00000652121.1:c.*109C>G | ENSP00000498314.1:n.*109C>G | |
| ENST00000300036.5:c.1926C>G | ENSP00000300036.5:p.Ala642= | |
| ENST00000396324.7:c.1947C>G | ENSP00000379616.3:p.Ala649= | |
| ENST00000452625.6:c.1947C>G | ENSP00000407821.2:p.Ala649= | |
| ENST00000570785.1:n.2348C>G | ||
| ENST00000576790.6:c.1926C>G | ENSP00000458731.1:p.Ala642= | |
| ENST00000616439.4:c.1947C>G | ENSP00000484924.1:p.Ala649= | |
| NM_001040113.1:c.1947C>G | NP_001035202.1:p.Ala649= | |
| NM_001040114.1:c.1947C>G | NP_001035203.1:p.Ala649= | |
| NM_002474.2:c.1926C>G | NP_002465.1:p.Ala642= | |
| NM_022844.2:c.1926C>G | NP_074035.1:p.Ala642= | |
| XM_011522502.1:c.1926C>G | XP_011520804.1:p.Ala642= | |
| XM_011522502.2:c.1926C>G | XP_011520804.1:p.Ala642= | |
| XM_017023250.1:c.1947C>G | XP_016878739.1:p.Ala649= | |
| NM_002474.3:c.1926C>G MANE Select | NP_002465.1:p.Ala642= | |
| NM_001040113.2:c.1947C>G MANE Plus Clinical | NP_001035202.1:p.Ala649= | |
| NM_001040114.2:c.1947C>G | NP_001035203.1:p.Ala649= | |
| NM_022844.3:c.1926C>G | NP_074035.1:p.Ala642= |