Linked Data
ClinVar Variation Id:
2006131
ClinVar RCV Id:
RCV002825733
MyVariant Identifiers:
chr5:g.7895870A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.7895757A>G , CM000667.2:g.7895757A>G | GRCh38 |
| NC_000005.9:g.7895870A>G , CM000667.1:g.7895870A>G | GRCh37 |
| NC_000005.8:g.7948870A>G | NCBI36 |
| NG_008856.1:g.31654A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000440940.7:c.1581A>G MANE Select | ENSP00000402510.2:p.Thr527= | |
| ENST00000264668.6:c.1662A>G | ENSP00000264668.2:p.Thr554= | |
| ENST00000440940.6:c.1581A>G | ENSP00000402510.2:p.Thr527= | |
| ENST00000510525.5:c.1517A>G | ||
| ENST00000511461.5:c.1494A>G | ||
| ENST00000513439.5:c.*1288A>G | ENSP00000426710.1:n.*1288A>G | |
| NM_002454.2:c.1581A>G | NP_002445.2:p.Thr527= | |
| NM_024010.2:c.1662A>G | NP_076915.2:p.Thr554= | |
| XM_011514043.1:c.1662A>G | XP_011512345.1:p.Thr554= | |
| XM_011514044.1:c.1581A>G | XP_011512346.1:p.Thr527= | |
| XR_241702.1:n.1595A>G | ||
| XR_241703.1:n.1588A>G | ||
| XR_925614.1:n.1707A>G | ||
| NM_001364440.1:c.1581A>G | NP_001351369.1:p.Thr527= | |
| NM_001364441.1:c.1581A>G | NP_001351370.1:p.Thr527= | |
| NM_001364442.1:c.1581A>G | NP_001351371.1:p.Thr527= | |
| NM_024010.3:c.1581A>G | NP_076915.3:p.Thr527= | |
| NR_134480.1:n.1704A>G | ||
| NR_134481.1:n.1629A>G | ||
| NR_134482.1:n.1564A>G | ||
| NR_157168.1:n.1634A>G | ||
| NR_157169.1:n.1494A>G | ||
| NR_157170.1:n.1660A>G | ||
| NR_157171.1:n.1517A>G | ||
| NR_157172.1:n.1431A>G | ||
| NR_157173.1:n.1671A>G | ||
| NR_157174.1:n.1672A>G | ||
| NR_157175.1:n.1826A>G | ||
| NR_157176.1:n.1989A>G | ||
| NR_157177.1:n.1669A>G | ||
| NR_157178.1:n.1697A>G | ||
| XM_024446063.1:c.1626A>G | XP_024301831.1:p.Thr542= | |
| XM_024446064.1:c.1581A>G | XP_024301832.1:p.Thr527= | |
| XR_001742071.1:n.1859A>G | ||
| XR_001742072.1:n.1836A>G | ||
| XR_001742074.1:n.1595A>G | ||
| XR_001742075.1:n.1747A>G | ||
| XR_001742076.1:n.1824A>G | ||
| XR_001742077.1:n.1847A>G | ||
| NM_001364440.2:c.1581A>G | NP_001351369.1:p.Thr527= | |
| NM_001364441.2:c.1581A>G | NP_001351370.1:p.Thr527= | |
| NM_001364442.2:c.1581A>G | NP_001351371.1:p.Thr527= | |
| NM_002454.3:c.1581A>G MANE Select | NP_002445.2:p.Thr527= | |
| NM_024010.4:c.1581A>G | NP_076915.3:p.Thr527= | |
| NR_134480.2:n.1660A>G | ||
| NR_134481.2:n.1585A>G | ||
| NR_134482.2:n.1520A>G | ||
| NR_157168.2:n.1634A>G | ||
| NR_157169.2:n.1494A>G | ||
| NR_157170.2:n.1660A>G | ||
| NR_157171.2:n.1517A>G | ||
| NR_157172.2:n.1431A>G | ||
| NR_157173.2:n.1671A>G | ||
| NR_157174.2:n.1672A>G | ||
| NR_157175.2:n.1826A>G | ||
| NR_157176.2:n.1989A>G | ||
| NR_157177.2:n.1669A>G | ||
| NR_157178.2:n.1697A>G |