Linked Data
ClinVar Variation Id:
2124481
ClinVar RCV Id:
RCV003057183
gnomAD v4:
7-107696025-C-T
MyVariant Identifiers:
chr7:g.107336470C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107696025C>T , CM000669.2:g.107696025C>T | GRCh38 |
| NC_000007.13:g.107336470C>T , CM000669.1:g.107336470C>T | GRCh37 |
| NC_000007.12:g.107123706C>T | NCBI36 |
| NG_008489.1:g.40391C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1530C>T MANE Select | ENSP00000494017.1:p.Val510= | |
| ENST00000644846.1:c.241C>T | ||
| ENST00000265715.7:c.1530C>T | ENSP00000265715.3:p.Val510= | |
| ENST00000477350.5:n.377C>T | ||
| ENST00000480841.5:n.379C>T | ||
| ENST00000497446.5:n.545C>T | ||
| NM_000441.1:c.1530C>T | NP_000432.1:p.Val510= | |
| XM_005250425.1:c.1530C>T | XP_005250482.1:p.Val510= | |
| XM_005250425.2:c.1530C>T | XP_005250482.1:p.Val510= | |
| XM_017012318.1:c.1452C>T | XP_016867807.1:p.Val484= | |
| NM_000441.2:c.1530C>T MANE Select | NP_000432.1:p.Val510= |