Linked Data
dbSNP Id:
rs1309834586
gnomAD v4:
9-4117891-G-C
MyVariant Identifiers:
chr9:g.4117891G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.4117891G>C , CM000671.2:g.4117891G>C | GRCh38 |
| NC_000009.11:g.4117891G>C , CM000671.1:g.4117891G>C | GRCh37 |
| NC_000009.10:g.4107891G>C | NCBI36 |
| NG_011782.1:g.187145C>G | |
| NG_011782.2:g.187145C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000491889.6:c.*950C>G | ENSP00000419914.1:n.*950C>G | |
| ENST00000645252.2:n.152+33049C>G | ||
| ENST00000682749.1:c.1122C>G | ENSP00000507306.1:p.Arg374= | |
| ENST00000682846.1:c.131+7843C>G | ENSP00000507527.1:n.131+7843C>G | |
| ENST00000381971.8:c.1587C>G MANE Select | ENSP00000371398.3:p.Arg529= | |
| ENST00000645252.1:n.152+33049C>G | ||
| ENST00000324333.14:c.1122C>G | ENSP00000325494.10:p.Arg374= | |
| ENST00000381971.7:c.1587C>G | ENSP00000371398.3:p.Arg529= | |
| ENST00000467497.6:n.127C>G | ||
| NM_001042413.1:c.1587C>G | NP_001035878.1:p.Arg529= | |
| NM_152629.3:c.1122C>G | NP_689842.3:p.Arg374= | |
| XM_005251386.3:c.1122C>G | XP_005251443.1:p.Arg374= | |
| XM_005251387.3:c.921C>G | XP_005251444.1:p.Arg307= | |
| XM_005251388.3:c.921C>G | XP_005251445.1:p.Arg307= | |
| XM_005251389.3:c.1587C>G | XP_005251446.1:p.Arg529= | |
| XM_006716731.2:c.1587C>G | XP_006716794.1:p.Arg529= | |
| XM_011517763.1:c.1587C>G | XP_011516065.1:p.Arg529= | |
| XM_011517764.1:c.1587C>G | XP_011516066.1:p.Arg529= | |
| XM_011517765.1:c.1587C>G | XP_011516067.1:p.Arg529= | |
| XM_011517766.1:c.1122C>G | XP_011516068.1:p.Arg374= | |
| XM_011517767.1:c.921C>G | XP_011516069.1:p.Arg307= | |
| XM_011517768.1:c.1587C>G | XP_011516070.1:p.Arg529= | |
| XM_011517769.1:c.1587C>G | XP_011516071.1:p.Arg529= | |
| XR_929206.1:n.2353C>G | ||
| XM_005251386.4:c.1122C>G | XP_005251443.1:p.Arg374= | |
| XM_005251387.4:c.921C>G | XP_005251444.1:p.Arg307= | |
| XM_005251388.4:c.921C>G | XP_005251445.1:p.Arg307= | |
| XM_005251389.5:c.1587C>G | XP_005251446.1:p.Arg529= | |
| XM_006716731.3:c.1587C>G | XP_006716794.1:p.Arg529= | |
| XM_011517763.2:c.1587C>G | XP_011516065.1:p.Arg529= | |
| XM_011517764.2:c.1587C>G | XP_011516066.1:p.Arg529= | |
| XM_011517765.2:c.1587C>G | XP_011516067.1:p.Arg529= | |
| XM_011517766.2:c.1122C>G | XP_011516068.1:p.Arg374= | |
| XM_011517767.3:c.921C>G | XP_011516069.1:p.Arg307= | |
| XM_011517769.2:c.1587C>G | XP_011516071.1:p.Arg529= | |
| XM_017014361.1:c.1122C>G | XP_016869850.1:p.Arg374= | |
| XR_929206.2:n.2349C>G | ||
| NM_001042413.2:c.1587C>G MANE Select | NP_001035878.1:p.Arg529= | |
| NM_152629.4:c.1122C>G | NP_689842.3:p.Arg374= |