Linked Data
dbSNP Id:
rs530216827
gnomAD v3:
20-46725342-C-A
gnomAD v4:
20-46725342-C-A
MyVariant Identifiers:
chr20:g.45353981C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46725342C>A , CM000682.2:g.46725342C>A | GRCh38 |
| NC_000020.10:g.45353981C>A , CM000682.1:g.45353981C>A | GRCh37 |
| NC_000020.9:g.44787388C>A | NCBI36 |
| NG_016284.1:g.20703C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000359271.4:c.306C>A MANE Select | ENSP00000352216.2:p.Val102= | |
| ENST00000359271.3:c.306C>A | ENSP00000352216.2:p.Val102= | |
| ENST00000611837.1:n.458C>A | ||
| NM_030777.3:c.306C>A | NP_110404.1:p.Val102= | |
| XM_011529060.1:c.369C>A | XP_011527362.1:p.Val123= | |
| XM_011529061.1:c.315C>A | XP_011527363.1:p.Val105= | |
| XM_011529062.1:c.369C>A | XP_011527364.1:p.Val123= | |
| XM_011529063.1:c.369C>A | XP_011527365.1:p.Val123= | |
| XM_011529064.1:c.369C>A | XP_011527366.1:p.Val123= | |
| XM_011529065.1:c.369C>A | XP_011527367.1:p.Val123= | |
| XR_936641.1:n.505C>A | ||
| XM_011529060.2:c.369C>A | XP_011527362.1:p.Val123= | |
| XM_011529061.2:c.315C>A | XP_011527363.1:p.Val105= | |
| XM_011529062.2:c.369C>A | XP_011527364.1:p.Val123= | |
| XM_011529063.2:c.369C>A | XP_011527365.1:p.Val123= | |
| XM_011529064.2:c.369C>A | XP_011527366.1:p.Val123= | |
| XM_011529065.2:c.369C>A | XP_011527367.1:p.Val123= | |
| XM_017028087.2:c.306C>A | XP_016883576.1:p.Val102= | |
| XR_936641.2:n.492C>A | ||
| NM_030777.4:c.306C>A MANE Select | NP_110404.1:p.Val102= |