Linked Data
ClinVar Variation Id:
199182
dbSNP Id:
rs555179389
ExAC:
5:36976401 T / A
gnomAD v2:
5-36976401-T-A
gnomAD v3:
5-36976299-T-A
gnomAD v4:
5-36976299-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.36976299T>A , CM000667.2:g.36976299T>A | GRCh38 |
| NC_000005.9:g.36976401T>A , CM000667.1:g.36976401T>A | GRCh37 |
| NC_000005.8:g.37012158T>A | NCBI36 |
| NG_006987.1:g.104417T>A | |
| NG_006987.2:g.104417T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000282516.13:c.1392T>A MANE Select | ENSP00000282516.8:p.Pro464= | |
| ENST00000652901.1:c.1392T>A | ENSP00000499536.1:p.Pro464= | |
| ENST00000282516.12:c.1392T>A | ENSP00000282516.8:p.Pro464= | |
| ENST00000448238.2:c.1392T>A | ENSP00000406266.2:p.Pro464= | |
| ENST00000504430.5:n.1012T>A | ||
| ENST00000621733.1:c.1-88279T>A | ENSP00000480694.1:n.1-88279T>A | |
| NM_015384.4:c.1392T>A | NP_056199.2:p.Pro464= | |
| NM_133433.3:c.1392T>A | NP_597677.2:p.Pro464= | |
| XM_005248280.2:c.1392T>A | XP_005248337.1:p.Pro464= | |
| XM_005248282.3:c.648T>A | XP_005248339.2:p.Pro216= | |
| XM_006714467.2:c.1392T>A | XP_006714530.1:p.Pro464= | |
| XM_006714468.1:c.1392T>A | XP_006714531.1:p.Pro464= | |
| XM_011514014.1:c.1392T>A | XP_011512316.1:p.Pro464= | |
| XM_011514015.1:c.1392T>A | XP_011512317.1:p.Pro464= | |
| XM_005248280.3:c.1392T>A | XP_005248337.1:p.Pro464= | |
| XM_005248282.5:c.732T>A | XP_005248339.3:p.Pro244= | |
| XM_006714468.2:c.1392T>A | XP_006714531.1:p.Pro464= | |
| XM_017009329.1:c.1392T>A | XP_016864818.1:p.Pro464= | |
| XM_017009331.1:c.1392T>A | XP_016864820.1:p.Pro464= | |
| NM_133433.4:c.1392T>A MANE Select | NP_597677.2:p.Pro464= | |
| NM_015384.5:c.1392T>A | NP_056199.2:p.Pro464= |