Linked Data
ClinVar Variation Id:
1419968
ClinVar RCV Id:
RCV001910757
dbSNP Id:
rs1801004397
gnomAD v4:
7-150948454-G-A
MyVariant Identifiers:
chr7:g.150645542G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150948454G>A , CM000669.2:g.150948454G>A | GRCh38 |
| NC_000007.13:g.150645542G>A , CM000669.1:g.150645542G>A | GRCh37 |
| NC_000007.12:g.150276475G>A | NCBI36 |
| NG_008916.1:g.34473C>T , LRG_288:g.34473C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684241.1:n.3515C>T | ||
| ENST00000262186.10:c.2682C>T MANE Select | ENSP00000262186.5:p.Arg894= | |
| ENST00000330883.9:c.1662C>T | ENSP00000328531.4:p.Arg554= | |
| ENST00000262186.9:c.2682C>T | ENSP00000262186.5:p.Arg894= | |
| ENST00000330883.8:c.1662C>T | ENSP00000328531.4:p.Arg554= | |
| NM_000238.3:c.2682C>T , LRG_288t1:c.2682C>T | NP_000229.1:p.Arg894= | |
| NM_172057.2:c.1662C>T , LRG_288t3:c.1662C>T | NP_742054.1:p.Arg554= | |
| XM_011516185.1:c.2382C>T | XP_011514487.1:p.Arg794= | |
| XM_011516186.1:c.2682C>T | XP_011514488.1:p.Arg894= | |
| XM_011516185.2:c.2382C>T | XP_011514487.1:p.Arg794= | |
| XM_011516186.3:c.2682C>T | XP_011514488.1:p.Arg894= | |
| XM_017012195.1:c.2532C>T | XP_016867684.1:p.Arg844= | |
| XM_017012196.1:c.2505C>T | XP_016867685.1:p.Arg835= | |
| NM_000238.4:c.2682C>T MANE Select | NP_000229.1:p.Arg894= | |
| NM_172057.3:c.1662C>T | NP_742054.1:p.Arg554= |