Linked Data
ClinVar Variation Id:
1093485
ClinVar RCV Id:
RCV001413672
dbSNP Id:
rs2117062260
MyVariant Identifiers:
chr7:g.150671818G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150974730G>T , CM000669.2:g.150974730G>T | GRCh38 |
| NC_000007.13:g.150671818G>T , CM000669.1:g.150671818G>T | GRCh37 |
| NC_000007.12:g.150302751G>T | NCBI36 |
| NG_008916.1:g.8197C>A , LRG_288:g.8197C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262186.10:c.288C>A MANE Select | ENSP00000262186.5:p.Ile96= | |
| ENST00000262186.9:c.288C>A | ENSP00000262186.5:p.Ile96= | |
| ENST00000430723.4:c.111C>A | ENSP00000387657.4:p.Ile37= | |
| ENST00000532957.5:n.511C>A | ||
| NM_000238.3:c.288C>A , LRG_288t1:c.288C>A | NP_000229.1:p.Ile96= | |
| NM_172056.2:c.288C>A , LRG_288t2:c.288C>A | NP_742053.1:p.Ile96= | |
| XM_011516186.1:c.288C>A | XP_011514488.1:p.Ile96= | |
| XM_011516186.3:c.288C>A | XP_011514488.1:p.Ile96= | |
| XM_017012196.1:c.111C>A | XP_016867685.1:p.Ile37= | |
| NM_000238.4:c.288C>A MANE Select | NP_000229.1:p.Ile96= |