Linked Data
ClinVar Variation Id:
889162
ClinVar RCV Id:
RCV001122929
dbSNP Id:
rs376504514
gnomAD v4:
17-7224366-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7224366C>T , CM000679.2:g.7224366C>T | GRCh38 |
| NC_000017.10:g.7127685C>T , CM000679.1:g.7127685C>T | GRCh37 |
| NC_000017.9:g.7068409C>T | NCBI36 |
| NG_007975.1:g.9533C>T | |
| NG_008391.2:g.685G>A | |
| NG_033038.1:g.15179G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1578C>T MANE Select | ENSP00000349297.5:p.His526= | |
| ENST00000322910.9:c.*1533C>T | ENSP00000325395.5:n.*1533C>T | |
| ENST00000350303.9:c.1512C>T | ENSP00000344152.5:p.His504= | |
| ENST00000356839.9:c.1578C>T | ENSP00000349297.5:p.His526= | |
| ENST00000542255.6:c.436C>T | ||
| ENST00000543245.6:c.1647C>T | ENSP00000438689.2:p.His549= | |
| ENST00000578319.5:n.73C>T | ||
| ENST00000578711.1:n.862C>T | ||
| ENST00000578809.5:n.150C>T | ||
| ENST00000579391.1:n.186C>T | ||
| ENST00000579425.5:n.694C>T | ||
| ENST00000579546.1:c.317C>T | ||
| ENST00000579894.5:n.365C>T | ||
| ENST00000582450.1:n.86C>T | ||
| ENST00000583074.5:n.199C>T | ||
| ENST00000583850.5:n.353C>T | ||
| ENST00000583858.5:c.509C>T | ||
| ENST00000585203.6:n.769C>T | ||
| NM_000018.3:c.1578C>T | NP_000009.1:p.His526= | |
| NM_001033859.2:c.1512C>T | NP_001029031.1:p.His504= | |
| NM_001270447.1:c.1647C>T | NP_001257376.1:p.His549= | |
| NM_001270448.1:c.1350C>T | NP_001257377.1:p.His450= | |
| XM_006721516.2:c.1578C>T | XP_006721579.2:p.His526= | |
| XM_011523829.1:c.1480C>T | XP_011522131.1:p.Pro494Ser | |
| XM_011523830.1:c.1480C>T | XP_011522132.1:p.Pro494Ser | |
| XR_934021.1:n.1685C>T | ||
| XR_934022.1:n.1587C>T | ||
| XR_934023.1:n.1587C>T | ||
| XM_006721516.3:c.1578C>T | XP_006721579.2:p.His526= | |
| XM_011523829.2:c.1480C>T | XP_011522131.1:p.Pro494Ser | |
| XM_011523830.2:c.1480C>T | XP_011522132.1:p.Pro494Ser | |
| XM_024450741.1:c.1480C>T | XP_024306509.1:p.Pro494Ser | |
| XR_934021.2:n.1637C>T | ||
| XR_934022.2:n.1539C>T | ||
| XR_934023.2:n.1539C>T | ||
| NM_000018.4:c.1578C>T MANE Select | NP_000009.1:p.His526= | |
| NM_001033859.3:c.1512C>T | NP_001029031.1:p.His504= | |
| NM_001270447.2:c.1647C>T | NP_001257376.1:p.His549= | |
| NM_001270448.2:c.1350C>T | NP_001257377.1:p.His450= |