Linked Data
ClinVar Variation Id:
928123
dbSNP Id:
rs1203403811
gnomAD v2:
7-150644001-G-C
gnomAD v3:
7-150946913-G-C
gnomAD v4:
7-150946913-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150946913G>C , CM000669.2:g.150946913G>C | GRCh38 |
| NC_000007.13:g.150644001G>C , CM000669.1:g.150644001G>C | GRCh37 |
| NC_000007.12:g.150274934G>C | NCBI36 |
| NG_008916.1:g.36014C>G , LRG_288:g.36014C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684241.1:n.4127C>G | ||
| ENST00000262186.10:c.3294C>G MANE Select | ENSP00000262186.5:p.Ser1098Arg | |
| ENST00000330883.9:c.2274C>G | ENSP00000328531.4:p.Ser758Arg | |
| ENST00000262186.9:c.3294C>G | ENSP00000262186.5:p.Ser1098Arg | |
| ENST00000330883.8:c.2274C>G | ENSP00000328531.4:p.Ser758Arg | |
| NM_000238.3:c.3294C>G , LRG_288t1:c.3294C>G | NP_000229.1:p.Ser1098Arg | |
| NM_172057.2:c.2274C>G , LRG_288t3:c.2274C>G | NP_742054.1:p.Ser758Arg | |
| XM_011516185.1:c.2994C>G | XP_011514487.1:p.Ser998Arg | |
| XM_011516185.2:c.2994C>G | XP_011514487.1:p.Ser998Arg | |
| XM_017012195.1:c.3144C>G | XP_016867684.1:p.Ser1048Arg | |
| XM_017012196.1:c.3117C>G | XP_016867685.1:p.Ser1039Arg | |
| NM_000238.4:c.3294C>G MANE Select | NP_000229.1:p.Ser1098Arg | |
| NM_172057.3:c.2274C>G | NP_742054.1:p.Ser758Arg |