Linked Data
ClinVar Variation Id:
239191
dbSNP Id:
rs6413508
ExAC:
8:90958423 G / A
gnomAD v2:
8-90958423-G-A
gnomAD v4:
8-89946195-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.89946195G>A , CM000670.2:g.89946195G>A | GRCh38 |
| NC_000008.10:g.90958423G>A , CM000670.1:g.90958423G>A | GRCh37 |
| NC_000008.9:g.91027599G>A | NCBI36 |
| NG_008860.1:g.43477C>T , LRG_158:g.43477C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494804.2:n.3317C>T | ||
| ENST00000517337.2:c.1769C>T | ENSP00000429971.2:p.Pro590Leu | |
| ENST00000523444.2:c.1769C>T | ENSP00000428252.2:p.Pro590Leu | |
| ENST00000697292.1:c.2015C>T | ENSP00000513229.1:p.Pro672Leu | |
| ENST00000697293.1:c.2015C>T | ENSP00000513230.1:p.Pro672Leu | |
| ENST00000697294.1:c.*1626C>T | ENSP00000513231.1:n.*1626C>T | |
| ENST00000697295.1:c.*1324C>T | ENSP00000513232.1:n.*1324C>T | |
| ENST00000697296.1:c.*1683C>T | ENSP00000513233.1:n.*1683C>T | |
| ENST00000697297.1:n.3800C>T | ||
| ENST00000697298.1:c.1769C>T | ENSP00000513234.1:p.Pro590Leu | |
| ENST00000697299.1:c.1769C>T | ENSP00000513235.1:p.Pro590Leu | |
| ENST00000697300.1:c.*1619C>T | ENSP00000513236.1:n.*1619C>T | |
| ENST00000697301.1:c.*1536C>T | ENSP00000513237.1:n.*1536C>T | |
| ENST00000697302.1:c.*1536C>T | ENSP00000513238.1:n.*1536C>T | |
| ENST00000697303.1:c.*1619C>T | ENSP00000513239.1:n.*1619C>T | |
| ENST00000697304.1:c.1703C>T | ENSP00000513240.1:p.Pro568Leu | |
| ENST00000697306.1:c.*2566C>T | ENSP00000513241.1:n.*2566C>T | |
| ENST00000697307.1:c.1846-2829C>T | ENSP00000513242.1:n.1846-2829C>T | |
| ENST00000697308.1:c.1946C>T | ENSP00000513243.1:p.Pro649Leu | |
| ENST00000697309.1:c.2015C>T | ENSP00000513244.1:p.Pro672Leu | |
| ENST00000697310.1:c.2015C>T | ENSP00000513245.1:p.Pro672Leu | |
| ENST00000697311.1:c.2015C>T | ENSP00000513246.1:p.Pro672Leu | |
| ENST00000697312.1:c.*1413C>T | ENSP00000513247.1:n.*1413C>T | |
| ENST00000697313.1:n.2688-10583C>T | ||
| ENST00000697314.1:n.3636+7049C>T | ||
| ENST00000697315.1:c.2015C>T | ENSP00000513248.1:p.Pro672Leu | |
| ENST00000697316.1:n.2136C>T | ||
| ENST00000697317.1:n.2106C>T | ||
| ENST00000265433.8:c.2015C>T MANE Select | ENSP00000265433.4:p.Pro672Leu | |
| ENST00000265433.7:c.2015C>T | ENSP00000265433.3:p.Pro672Leu | |
| ENST00000396252.6:c.*1888C>T | ENSP00000379551.2:n.*1888C>T | |
| ENST00000409330.5:c.1769C>T | ENSP00000386924.1:p.Pro590Leu | |
| ENST00000520325.1:n.431C>T | ||
| ENST00000613033.1:c.180+1629C>T | ENSP00000484487.1:n.180+1629C>T | |
| NM_001024688.2:c.1769C>T | NP_001019859.1:p.Pro590Leu | |
| NM_002485.4:c.2015C>T , LRG_158t1:c.2015C>T | NP_002476.2:p.Pro672Leu | |
| XM_011517044.1:c.1991C>T | XP_011515346.1:p.Pro664Leu | |
| XM_011517045.1:c.1769C>T | XP_011515347.1:p.Pro590Leu | |
| XM_017013460.1:c.1136C>T | XP_016868949.1:p.Pro379Leu | |
| XM_017013462.2:c.1136C>T | XP_016868951.1:p.Pro379Leu | |
| XM_024447163.1:c.1769C>T | XP_024302931.1:p.Pro590Leu | |
| XM_024447164.1:c.1769C>T | XP_024302932.1:p.Pro590Leu | |
| XM_024447165.1:c.1136C>T | XP_024302933.1:p.Pro379Leu | |
| NM_002485.5:c.2015C>T MANE Select | NP_002476.2:p.Pro672Leu | |
| NM_001024688.3:c.1769C>T | NP_001019859.1:p.Pro590Leu |