Linked Data
ClinVar Variation Id:
2033119
ClinVar RCV Id:
RCV002881684
MyVariant Identifiers:
chr17:g.7123976G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7220657G>A , CM000679.2:g.7220657G>A | GRCh38 |
| NC_000017.10:g.7123976G>A , CM000679.1:g.7123976G>A | GRCh37 |
| NC_000017.9:g.7064700G>A | NCBI36 |
| NG_007975.1:g.5824G>A | |
| NG_008391.2:g.4394C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.258G>A MANE Select | ENSP00000349297.5:p.Gln86= | |
| ENST00000322910.9:c.*213G>A | ENSP00000325395.5:n.*213G>A | |
| ENST00000350303.9:c.192G>A | ENSP00000344152.5:p.Gln64= | |
| ENST00000356839.9:c.258G>A | ENSP00000349297.5:p.Gln86= | |
| ENST00000543245.6:c.327G>A | ENSP00000438689.2:p.Gln109= | |
| ENST00000577191.5:n.335G>A | ||
| ENST00000577433.5:n.466G>A | ||
| ENST00000577857.5:n.229-109G>A | ||
| ENST00000578269.5:n.705G>A | ||
| ENST00000578421.1:n.466G>A | ||
| ENST00000579286.5:n.439G>A | ||
| ENST00000579886.2:c.201+131G>A | ENSP00000463246.1:n.201+131G>A | |
| ENST00000580263.5:n.422G>A | ||
| ENST00000581562.5:n.305G>A | ||
| ENST00000582056.5:n.348G>A | ||
| ENST00000582166.1:n.146G>A | ||
| ENST00000582356.5:n.457G>A | ||
| ENST00000583312.5:c.258G>A | ENSP00000467920.1:p.Gln86= | |
| ENST00000584103.5:c.258G>A | ENSP00000465353.1:p.Gln86= | |
| NM_000018.3:c.258G>A | NP_000009.1:p.Gln86= | |
| NM_001033859.2:c.192G>A | NP_001029031.1:p.Gln64= | |
| NM_001270447.1:c.327G>A | NP_001257376.1:p.Gln109= | |
| NM_001270448.1:c.30G>A | NP_001257377.1:p.Gln10= | |
| XM_006721516.2:c.258G>A | XP_006721579.2:p.Gln86= | |
| XM_011523829.1:c.258G>A | XP_011522131.1:p.Gln86= | |
| XM_011523830.1:c.258G>A | XP_011522132.1:p.Gln86= | |
| XR_934021.1:n.365G>A | ||
| XR_934022.1:n.365G>A | ||
| XR_934023.1:n.365G>A | ||
| XM_006721516.3:c.258G>A | XP_006721579.2:p.Gln86= | |
| XM_011523829.2:c.258G>A | XP_011522131.1:p.Gln86= | |
| XM_011523830.2:c.258G>A | XP_011522132.1:p.Gln86= | |
| XM_024450741.1:c.258G>A | XP_024306509.1:p.Gln86= | |
| XR_934021.2:n.317G>A | ||
| XR_934022.2:n.317G>A | ||
| XR_934023.2:n.317G>A | ||
| NM_000018.4:c.258G>A MANE Select | NP_000009.1:p.Gln86= | |
| NM_001033859.3:c.192G>A | NP_001029031.1:p.Gln64= | |
| NM_001270447.2:c.327G>A | NP_001257376.1:p.Gln109= | |
| NM_001270448.2:c.30G>A | NP_001257377.1:p.Gln10= |