Linked Data
ClinVar Variation Id:
499392
dbSNP Id:
rs775297789
ExAC:
1:10683102 C / T
gnomAD v2:
1-10683102-C-T
gnomAD v3:
1-10623045-C-T
gnomAD v4:
1-10623045-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.10623045C>T , CM000663.2:g.10623045C>T | GRCh38 |
| NC_000001.10:g.10683102C>T , CM000663.1:g.10683102C>T | GRCh37 |
| NC_000001.9:g.10605689C>T | NCBI36 |
| NG_008340.1:g.153100C>T | |
| NG_008340.2:g.153100C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356607.9:c.411C>T MANE Select | ENSP00000349016.4:p.Gly137= | |
| ENST00000356607.8:c.411C>T | ENSP00000349016.4:p.Gly137= | |
| ENST00000491661.2:c.396C>T | ENSP00000465473.1:p.Gly132= | |
| NM_004565.2:c.411C>T | NP_004556.1:p.Gly137= | |
| XM_005263470.3:c.219C>T | XP_005263527.1:p.Gly73= | |
| XM_011541577.1:c.453C>T | XP_011539879.1:p.Gly151= | |
| XM_011541578.1:c.354C>T | XP_011539880.1:p.Gly118= | |
| XM_011541579.1:c.324C>T | XP_011539881.1:p.Gly108= | |
| XM_011541580.1:c.282C>T | XP_011539882.1:p.Gly94= | |
| XM_005263470.5:c.219C>T | XP_005263527.1:p.Gly73= | |
| XM_011541577.2:c.453C>T | XP_011539879.1:p.Gly151= | |
| XM_011541578.2:c.354C>T | XP_011539880.1:p.Gly118= | |
| XM_011541579.3:c.324C>T | XP_011539881.1:p.Gly108= | |
| XM_024447651.1:c.219C>T | XP_024303419.1:p.Gly73= | |
| NM_004565.3:c.411C>T MANE Select | NP_004556.1:p.Gly137= |