Linked Data
dbSNP Id:
rs766370306
ExAC:
20:948695 G / A
gnomAD v2:
20-948695-G-A
gnomAD v4:
20-968052-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.968052G>A , CM000682.2:g.968052G>A | GRCh38 |
| NC_000020.10:g.948695G>A , CM000682.1:g.948695G>A | GRCh37 |
| NC_000020.9:g.896695G>A | NCBI36 |
| NG_013043.1:g.39213C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217260.9:c.166C>T MANE Select | ENSP00000217260.4:p.Leu56= | |
| ENST00000217260.8:c.166C>T | ENSP00000217260.4:p.Leu56= | |
| ENST00000400634.2:c.166C>T | ENSP00000383475.2:p.Leu56= | |
| NM_001029871.3:c.166C>T | NP_001025042.2:p.Leu56= | |
| NM_001040007.2:c.166C>T | NP_001035096.1:p.Leu56= | |
| XM_011529232.1:c.214C>T | XP_011527534.1:p.Leu72= | |
| XM_011529233.1:c.214C>T | XP_011527535.1:p.Leu72= | |
| XR_937068.1:n.286C>T | ||
| XR_937069.1:n.281C>T | ||
| XM_017027839.1:c.166C>T | XP_016883328.1:p.Leu56= | |
| NM_001029871.4:c.166C>T MANE Select | NP_001025042.2:p.Leu56= | |
| NM_001040007.3:c.166C>T | NP_001035096.1:p.Leu56= |