Linked Data
ClinVar Variation Id:
155732
ClinVar RCV Id:
RCV000143801
dbSNP Id:
rs587777890
gnomAD v4:
12-109793944-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.109793944A>C , CM000674.2:g.109793944A>C | GRCh38 |
| NC_000012.11:g.110231749A>C , CM000674.1:g.110231749A>C | GRCh37 |
| NC_000012.10:g.108716132A>C | NCBI36 |
| NG_017090.1:g.44464T>G , LRG_372:g.44464T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261740.7:c.1570T>G MANE Select | ENSP00000261740.2:p.Phe524Val | |
| ENST00000418703.7:c.1570T>G | ENSP00000406191.2:p.Phe524Val | |
| ENST00000674908.1:c.*657T>G | ENSP00000502012.1:n.*657T>G | |
| ENST00000675533.1:n.1601T>G | ||
| ENST00000675670.1:c.1570T>G | ENSP00000502135.1:p.Phe524Val | |
| ENST00000676376.1:n.1601T>G | ||
| ENST00000261740.6:c.1570T>G | ENSP00000261740.2:p.Phe524Val | |
| ENST00000418703.6:c.1570T>G | ENSP00000406191.2:p.Phe524Val | |
| ENST00000536838.1:c.1468T>G | ENSP00000444336.1:p.Phe490Val | |
| ENST00000537083.5:c.1390T>G | ENSP00000442738.1:p.Phe464Val | |
| ENST00000538125.5:c.1570T>G | ENSP00000437449.1:p.Phe524Val | |
| ENST00000541794.5:c.1429T>G | ENSP00000442167.1:p.Phe477Val | |
| ENST00000544971.5:c.1249T>G | ENSP00000443611.1:p.Phe417Val | |
| NM_001177428.1:c.1429T>G | NP_001170899.1:p.Phe477Val | |
| NM_001177431.1:c.1468T>G | NP_001170902.1:p.Phe490Val | |
| NM_001177433.1:c.1249T>G | NP_001170904.1:p.Phe417Val | |
| NM_021625.4:c.1570T>G , LRG_372t1:c.1570T>G | NP_067638.3:p.Phe524Val | |
| NM_147204.2:c.1390T>G | NP_671737.1:p.Phe464Val | |
| XM_005253918.1:c.1570T>G | XP_005253975.1:p.Phe524Val | |
| XM_011538630.1:c.1570T>G | XP_011536932.1:p.Phe524Val | |
| XM_011538631.1:c.1429T>G | XP_011536933.1:p.Phe477Val | |
| XM_011538632.1:c.1390T>G | XP_011536934.1:p.Phe464Val | |
| XM_011538633.1:c.1249T>G | XP_011536935.1:p.Phe417Val | |
| XM_011538634.1:c.1570T>G | XP_011536936.1:p.Phe524Val | |
| XM_011538635.1:c.1723T>G | XP_011536937.1:p.Phe575Val | |
| XM_011538636.1:c.1723T>G | XP_011536938.1:p.Phe575Val | |
| XM_011538630.2:c.1723T>G | XP_011536932.2:p.Phe575Val | |
| XM_011538631.2:c.1582T>G | XP_011536933.2:p.Phe528Val | |
| XM_011538632.2:c.1543T>G | XP_011536934.2:p.Phe515Val | |
| XM_011538633.2:c.1402T>G | XP_011536935.2:p.Phe468Val | |
| XM_011538634.2:c.1723T>G | XP_011536936.2:p.Phe575Val | |
| XM_011538635.2:c.1723T>G | XP_011536937.1:p.Phe575Val | |
| XM_017019774.1:c.1570T>G | XP_016875263.1:p.Phe524Val | |
| NM_021625.5:c.1570T>G MANE Select | NP_067638.3:p.Phe524Val |