Linked Data
ClinVar Variation Id:
457644
dbSNP Id:
rs902739109
gnomAD v2:
17-29559777-C-T
gnomAD v4:
17-31232759-C-T
PubMed:
PMID:10336779
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.31232759C>T , CM000679.2:g.31232759C>T | GRCh38 |
| NC_000017.10:g.29559777C>T , CM000679.1:g.29559777C>T | GRCh37 |
| NC_000017.9:g.26583903C>T | NCBI36 |
| NG_009018.1:g.142783C>T , LRG_214:g.142783C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696138.1:c.3419C>T | ENSP00000512431.1:p.Ala1140Val | |
| ENST00000696139.1:c.719C>T | ENSP00000512432.1:p.Ala240Val | |
| ENST00000691014.1:c.3404C>T | ENSP00000510595.1:p.Ala1135Val | |
| ENST00000693210.1:n.100C>T | ||
| ENST00000358273.9:c.3374C>T MANE Select | ENSP00000351015.4:p.Ala1125Val | |
| ENST00000356175.7:c.3374C>T | ENSP00000348498.3:p.Ala1125Val | |
| ENST00000358273.8:c.3374C>T | ENSP00000351015.4:p.Ala1125Val | |
| ENST00000456735.6:c.2372C>T | ENSP00000389907.2:p.Ala791Val | |
| ENST00000493220.5:n.1910C>T | ||
| ENST00000495910.6:c.3149C>T | ||
| ENST00000579081.5:c.3476C>T | ENSP00000462408.1:p.Ala1159Val | |
| NM_000267.3:c.3374C>T , LRG_214t1:c.3374C>T | NP_000258.1:p.Ala1125Val | |
| NM_001042492.2:c.3374C>T , LRG_214t2:c.3374C>T | NP_001035957.1:p.Ala1125Val | |
| XM_005257983.1:c.3374C>T | XP_005258040.1:p.Ala1125Val | |
| XM_005257984.1:c.3374C>T | XP_005258041.1:p.Ala1125Val | |
| XM_006721922.1:c.3404C>T | XP_006721985.1:p.Ala1135Val | |
| XM_006721923.2:c.3365C>T | XP_006721986.1:p.Ala1122Val | |
| XM_006721924.1:c.3404C>T | XP_006721987.1:p.Ala1135Val | |
| XM_006721925.1:c.3404C>T | XP_006721988.1:p.Ala1135Val | |
| XM_006721926.2:c.3404C>T | XP_006721989.1:p.Ala1135Val | |
| XM_006721927.1:c.3404C>T | XP_006721990.1:p.Ala1135Val | |
| XM_006721928.2:c.3404C>T | XP_006721991.1:p.Ala1135Val | |
| XM_011524852.1:c.3401C>T | XP_011523154.1:p.Ala1134Val | |
| XM_011524853.1:c.3365C>T | XP_011523155.1:p.Ala1122Val | |
| XM_011524854.1:c.3365C>T | XP_011523156.1:p.Ala1122Val | |
| XM_011524855.1:c.3365C>T | XP_011523157.1:p.Ala1122Val | |
| XM_011524856.1:c.3365C>T | XP_011523158.1:p.Ala1122Val | |
| XM_011524857.1:c.3404C>T | XP_011523159.1:p.Ala1135Val | |
| NM_001042492.3:c.3374C>T MANE Select | NP_001035957.1:p.Ala1125Val |