Linked Data
ClinVar Variation Id:
3075421
ClinVar RCV Id:
RCV004016939
MyVariant Identifiers:
chr7:g.150647287G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150950199G>A , CM000669.2:g.150950199G>A | GRCh38 |
| NC_000007.13:g.150647287G>A , CM000669.1:g.150647287G>A | GRCh37 |
| NC_000007.12:g.150278220G>A | NCBI36 |
| NG_008916.1:g.32728C>T , LRG_288:g.32728C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461280.2:n.1665C>T | ||
| ENST00000684241.1:n.3200C>T | ||
| ENST00000262186.10:c.2367C>T MANE Select | ENSP00000262186.5:p.Ile789= | |
| ENST00000330883.9:c.1347C>T | ENSP00000328531.4:p.Ile449= | |
| ENST00000262186.9:c.2367C>T | ENSP00000262186.5:p.Ile789= | |
| ENST00000330883.8:c.1347C>T | ENSP00000328531.4:p.Ile449= | |
| ENST00000430723.4:c.2019C>T | ENSP00000387657.4:p.Ile673= | |
| ENST00000461280.1:n.1654C>T | ||
| ENST00000473610.5:n.1999C>T | ||
| ENST00000532957.5:n.2590C>T | ||
| NM_000238.3:c.2367C>T , LRG_288t1:c.2367C>T | NP_000229.1:p.Ile789= | |
| NM_001204798.1:c.1347C>T | NP_001191727.1:p.Ile449= | |
| NM_172056.2:c.2367C>T , LRG_288t2:c.2367C>T | NP_742053.1:p.Ile789= | |
| NM_172057.2:c.1347C>T , LRG_288t3:c.1347C>T | NP_742054.1:p.Ile449= | |
| XM_011516185.1:c.2067C>T | XP_011514487.1:p.Ile689= | |
| XM_011516186.1:c.2367C>T | XP_011514488.1:p.Ile789= | |
| XM_011516185.2:c.2067C>T | XP_011514487.1:p.Ile689= | |
| XM_011516186.3:c.2367C>T | XP_011514488.1:p.Ile789= | |
| XM_017012195.1:c.2217C>T | XP_016867684.1:p.Ile739= | |
| XM_017012196.1:c.2190C>T | XP_016867685.1:p.Ile730= | |
| NM_000238.4:c.2367C>T MANE Select | NP_000229.1:p.Ile789= | |
| NM_001204798.2:c.1347C>T | NP_001191727.1:p.Ile449= | |
| NM_172057.3:c.1347C>T | NP_742054.1:p.Ile449= |