Linked Data
ClinVar Variation Id:
1353839
ClinVar RCV Id:
RCV001863627
dbSNP Id:
rs1450189149
gnomAD v2:
8-90994975-G-A
gnomAD v4:
8-89982747-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.89982747G>A , CM000670.2:g.89982747G>A | GRCh38 |
| NC_000008.10:g.90994975G>A , CM000670.1:g.90994975G>A | GRCh37 |
| NC_000008.9:g.91064151G>A | NCBI36 |
| NG_008860.1:g.6925C>T , LRG_158:g.6925C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494804.2:n.250C>T | ||
| ENST00000517337.2:c.-151C>T | ENSP00000429971.2:n.-151C>T | |
| ENST00000523444.2:c.-151C>T | ENSP00000428252.2:n.-151C>T | |
| ENST00000697292.1:c.146C>T | ENSP00000513229.1:p.Thr49Ile | |
| ENST00000697293.1:c.146C>T | ENSP00000513230.1:p.Thr49Ile | |
| ENST00000697294.1:c.146C>T | ENSP00000513231.1:p.Thr49Ile | |
| ENST00000697295.1:c.37+1778C>T | ENSP00000513232.1:n.37+1778C>T | |
| ENST00000697296.1:c.146C>T | ENSP00000513233.1:p.Thr49Ile | |
| ENST00000697297.1:n.252C>T | ||
| ENST00000697298.1:c.-151C>T | ENSP00000513234.1:n.-151C>T | |
| ENST00000697299.1:c.-75-1224C>T | ENSP00000513235.1:n.-75-1224C>T | |
| ENST00000697300.1:c.-151C>T | ENSP00000513236.1:n.-151C>T | |
| ENST00000697301.1:c.-151C>T | ENSP00000513237.1:n.-151C>T | |
| ENST00000697302.1:c.146C>T | ENSP00000513238.1:p.Thr49Ile | |
| ENST00000697303.1:c.146C>T | ENSP00000513239.1:p.Thr49Ile | |
| ENST00000697304.1:c.146C>T | ENSP00000513240.1:p.Thr49Ile | |
| ENST00000697306.1:c.146C>T | ENSP00000513241.1:p.Thr49Ile | |
| ENST00000697307.1:c.146C>T | ENSP00000513242.1:p.Thr49Ile | |
| ENST00000697308.1:c.146C>T | ENSP00000513243.1:p.Thr49Ile | |
| ENST00000697309.1:c.146C>T | ENSP00000513244.1:p.Thr49Ile | |
| ENST00000697310.1:c.146C>T | ENSP00000513245.1:p.Thr49Ile | |
| ENST00000697311.1:c.146C>T | ENSP00000513246.1:p.Thr49Ile | |
| ENST00000697312.1:c.146C>T | ENSP00000513247.1:p.Thr49Ile | |
| ENST00000697313.1:n.258C>T | ||
| ENST00000697314.1:n.258C>T | ||
| ENST00000697315.1:c.146C>T | ENSP00000513248.1:p.Thr49Ile | |
| ENST00000697316.1:n.267C>T | ||
| ENST00000697317.1:n.256C>T | ||
| ENST00000697318.1:n.258C>T | ||
| ENST00000265433.8:c.146C>T MANE Select | ENSP00000265433.4:p.Thr49Ile | |
| ENST00000265433.7:c.146C>T | ENSP00000265433.3:p.Thr49Ile | |
| ENST00000396252.6:c.146C>T | ENSP00000379551.2:p.Thr49Ile | |
| ENST00000409330.5:c.-101C>T | ENSP00000386924.1:n.-101C>T | |
| ENST00000494804.1:n.250C>T | ||
| ENST00000517337.1:c.-151C>T | ENSP00000429971.1:n.-151C>T | |
| ENST00000519426.5:c.146C>T | ENSP00000430983.1:p.Thr49Ile | |
| ENST00000523444.1:c.146C>T | ENSP00000428252.1:p.Thr49Ile | |
| NM_001024688.2:c.-151C>T | NP_001019859.1:n.-151C>T | |
| NM_002485.4:c.146C>T , LRG_158t1:c.146C>T | NP_002476.2:p.Thr49Ile | |
| XM_011517044.1:c.122C>T | XP_011515346.1:p.Thr41Ile | |
| XM_011517045.1:c.-151C>T | XP_011515347.1:n.-151C>T | |
| XM_011517046.1:c.146C>T | XP_011515348.1:p.Thr49Ile | |
| XR_928335.1:n.283C>T | ||
| XM_017013460.1:c.-874C>T | XP_016868949.1:n.-874C>T | |
| XM_017013462.2:c.-680C>T | XP_016868951.1:n.-680C>T | |
| XM_024447163.1:c.-101C>T | XP_024302931.1:n.-101C>T | |
| XM_024447165.1:c.-824C>T | XP_024302933.1:n.-824C>T | |
| NM_002485.5:c.146C>T MANE Select | NP_002476.2:p.Thr49Ile | |
| NM_001024688.3:c.-151C>T | NP_001019859.1:n.-151C>T |