Linked Data
ClinVar Variation Id:
473389
dbSNP Id:
rs372410150
ExAC:
9:138678252 C / T
gnomAD v2:
9-138678252-C-T
gnomAD v3:
9-135786406-C-T
gnomAD v4:
9-135786406-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135786406C>T , CM000671.2:g.135786406C>T | GRCh38 |
| NC_000009.11:g.138678252C>T , CM000671.1:g.138678252C>T | GRCh37 |
| NC_000009.10:g.137818073C>T | NCBI36 |
| NG_033070.1:g.89222C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371757.7:c.3387C>T MANE Select | ENSP00000360822.2:p.Ala1129= | |
| ENST00000674572.1:c.3228C>T | ENSP00000501742.1:p.Ala1076= | |
| ENST00000675090.1:c.3135C>T | ENSP00000501833.1:p.Ala1045= | |
| ENST00000675399.1:c.3135C>T | ENSP00000501932.1:p.Ala1045= | |
| ENST00000676421.1:c.3144C>T | ENSP00000502322.1:p.Ala1048= | |
| ENST00000263604.5:c.3288C>T | ENSP00000263604.4:p.Ala1096= | |
| ENST00000371757.6:c.3387C>T | ENSP00000360822.2:p.Ala1129= | |
| ENST00000460750.5:c.*2997C>T | ENSP00000418777.1:n.*2997C>T | |
| ENST00000486577.6:c.3270C>T | ENSP00000417578.3:p.Ala1090= | |
| ENST00000487664.5:c.3387C>T | ENSP00000417851.2:p.Ala1129= | |
| ENST00000488444.6:c.3309C>T | ENSP00000419007.3:p.Ala1103= | |
| ENST00000490355.6:c.3324C>T | ENSP00000418003.3:p.Ala1108= | |
| ENST00000491806.6:c.3330C>T | ENSP00000419086.3:p.Ala1110= | |
| ENST00000628528.2:c.3252C>T | ENSP00000486374.1:p.Ala1084= | |
| ENST00000630792.2:c.3222C>T | ENSP00000486486.1:p.Ala1074= | |
| ENST00000631073.2:c.3330C>T | ENSP00000486130.1:p.Ala1110= | |
| NM_001272003.1:c.3252C>T | NP_001258932.1:p.Ala1084= | |
| NM_020822.2:c.3387C>T | NP_065873.2:p.Ala1129= | |
| XM_011518877.1:c.3522C>T | XP_011517179.1:p.Ala1174= | |
| XM_011518878.1:c.3531C>T | XP_011517180.1:p.Ala1177= | |
| XM_011518879.1:c.3522C>T | XP_011517181.1:p.Ala1174= | |
| XM_011518880.1:c.3288C>T | XP_011517182.1:p.Ala1096= | |
| XM_011518881.1:c.2877C>T | XP_011517183.1:p.Ala959= | |
| XM_011518877.3:c.3522C>T | XP_011517179.1:p.Ala1174= | |
| XM_011518878.3:c.3531C>T | XP_011517180.1:p.Ala1177= | |
| XM_011518879.3:c.3522C>T | XP_011517181.1:p.Ala1174= | |
| XM_011518881.3:c.2877C>T | XP_011517183.1:p.Ala959= | |
| XM_017014931.1:c.3321C>T | XP_016870420.1:p.Ala1107= | |
| XM_017014932.1:c.3144C>T | XP_016870421.1:p.Ala1048= | |
| XM_017014933.1:c.2877C>T | XP_016870422.1:p.Ala959= | |
| XM_024447617.1:c.2877C>T | XP_024303385.1:p.Ala959= | |
| XM_024447618.1:c.2877C>T | XP_024303386.1:p.Ala959= | |
| NM_020822.3:c.3387C>T MANE Select | NP_065873.2:p.Ala1129= | |
| NM_001272003.2:c.3252C>T | NP_001258932.1:p.Ala1084= |