Linked Data
ClinVar Variation Id:
3073371
ClinVar RCV Id:
RCV004016377
dbSNP Id:
rs770899326
gnomAD v2:
7-150649654-G-C
gnomAD v4:
7-150952566-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150952566G>C , CM000669.2:g.150952566G>C | GRCh38 |
| NC_000007.13:g.150649654G>C , CM000669.1:g.150649654G>C | GRCh37 |
| NC_000007.12:g.150280587G>C | NCBI36 |
| NG_008916.1:g.30361C>G , LRG_288:g.30361C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461280.2:n.714C>G | ||
| ENST00000684116.1:n.309C>G | ||
| ENST00000684241.1:n.2249C>G | ||
| ENST00000262186.10:c.1416C>G MANE Select | ENSP00000262186.5:p.Arg472= | |
| ENST00000330883.9:c.396C>G | ENSP00000328531.4:p.Arg132= | |
| ENST00000262186.9:c.1416C>G | ENSP00000262186.5:p.Arg472= | |
| ENST00000330883.8:c.396C>G | ENSP00000328531.4:p.Arg132= | |
| ENST00000430723.4:c.1068C>G | ENSP00000387657.4:p.Arg356= | |
| ENST00000461280.1:n.703C>G | ||
| ENST00000473610.5:n.721C>G | ||
| ENST00000532957.5:n.1639C>G | ||
| NM_000238.3:c.1416C>G , LRG_288t1:c.1416C>G | NP_000229.1:p.Arg472= | |
| NM_001204798.1:c.396C>G | NP_001191727.1:p.Arg132= | |
| NM_172056.2:c.1416C>G , LRG_288t2:c.1416C>G | NP_742053.1:p.Arg472= | |
| NM_172057.2:c.396C>G , LRG_288t3:c.396C>G | NP_742054.1:p.Arg132= | |
| XM_011516185.1:c.1116C>G | XP_011514487.1:p.Arg372= | |
| XM_011516186.1:c.1416C>G | XP_011514488.1:p.Arg472= | |
| XM_011516185.2:c.1116C>G | XP_011514487.1:p.Arg372= | |
| XM_011516186.3:c.1416C>G | XP_011514488.1:p.Arg472= | |
| XM_017012195.1:c.1266C>G | XP_016867684.1:p.Arg422= | |
| XM_017012196.1:c.1239C>G | XP_016867685.1:p.Arg413= | |
| NM_000238.4:c.1416C>G MANE Select | NP_000229.1:p.Arg472= | |
| NM_001204798.2:c.396C>G | NP_001191727.1:p.Arg132= | |
| NM_172057.3:c.396C>G | NP_742054.1:p.Arg132= |