Linked Data
dbSNP Id:
rs771792088
ExAC:
9:94486059 T / C
gnomAD v2:
9-94486059-T-C
gnomAD v4:
9-91723777-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.91723777T>C , CM000671.2:g.91723777T>C | GRCh38 |
| NC_000009.11:g.94486059T>C , CM000671.1:g.94486059T>C | GRCh37 |
| NC_000009.10:g.93525880T>C | NCBI36 |
| NG_008089.1:g.231386A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375708.4:c.2717A>G MANE Select | ENSP00000364860.3:p.Gln906Arg | |
| ENST00000375708.3:c.2717A>G | ENSP00000364860.3:p.Gln906Arg | |
| ENST00000375715.5:c.1920+377A>G | ENSP00000364867.1:n.1920+377A>G | |
| ENST00000550066.5:n.3185A>G | ||
| NM_004560.3:c.2717A>G | NP_004551.2:p.Gln906Arg | |
| XM_005252008.3:c.2297A>G | XP_005252065.1:p.Gln766Arg | |
| XM_005252009.3:c.1514A>G | XP_005252066.1:p.Gln505Arg | |
| XM_006717121.2:c.2297A>G | XP_006717184.1:p.Gln766Arg | |
| XM_011518721.1:c.2297A>G | XP_011517023.1:p.Gln766Arg | |
| XM_005252008.4:c.2297A>G | XP_005252065.1:p.Gln766Arg | |
| XM_006717121.3:c.2297A>G | XP_006717184.1:p.Gln766Arg | |
| XM_017014762.1:c.2708A>G | XP_016870251.1:p.Gln903Arg | |
| XM_017014763.1:c.2297A>G | XP_016870252.1:p.Gln766Arg | |
| NM_004560.4:c.2717A>G MANE Select | NP_004551.2:p.Gln906Arg |