Linked Data
dbSNP Id:
rs2063719124
gnomAD v4:
20-44419806-G-T
MyVariant Identifiers:
chr20:g.43048446G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44419806G>T , CM000682.2:g.44419806G>T | GRCh38 |
| NC_000020.10:g.43048446G>T , CM000682.1:g.43048446G>T | GRCh37 |
| NC_000020.9:g.42481860G>T | NCBI36 |
| NG_009818.1:g.69006G>T , LRG_483:g.69006G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316673.9:c.756G>T MANE Select | ENSP00000315180.4:p.Leu252= | |
| ENST00000316099.10:c.822G>T | ENSP00000312987.3:p.Leu274= | |
| ENST00000619550.5:c.796G>T | ||
| ENST00000683148.1:n.798G>T | ||
| ENST00000683657.1:n.1946G>T | ||
| ENST00000316099.9:c.822G>T | ENSP00000312987.3:p.Leu274= | |
| ENST00000316099.8:c.822G>T | ENSP00000312987.3:p.Leu274= | |
| ENST00000316673.8:c.756G>T | ENSP00000315180.4:p.Leu252= | |
| ENST00000372920.1:c.*589G>T | ENSP00000362011.1:n.*589G>T | |
| ENST00000415691.2:c.822G>T | ENSP00000412111.1:p.Leu274= | |
| ENST00000443598.6:c.822G>T | ENSP00000410911.2:p.Leu274= | |
| ENST00000457232.5:c.756G>T | ENSP00000396216.1:p.Leu252= | |
| ENST00000609795.5:c.756G>T | ENSP00000476609.1:p.Leu252= | |
| ENST00000619550.4:c.747G>T | ENSP00000481331.1:p.Leu249= | |
| NM_000457.4:c.822G>T , LRG_483t2:c.822G>T | NP_000448.3:p.Leu274= | |
| NM_001030003.2:c.756G>T | NP_001025174.1:p.Leu252= | |
| NM_001030004.2:c.756G>T | NP_001025175.1:p.Leu252= | |
| NM_001258355.1:c.801G>T | NP_001245284.1:p.Leu267= | |
| NM_001287182.1:c.747G>T | NP_001274111.1:p.Leu249= | |
| NM_001287183.1:c.747G>T , LRG_483t3:c.747G>T | NP_001274112.1:p.Leu249= | |
| NM_001287184.1:c.747G>T | NP_001274113.1:p.Leu249= | |
| NM_175914.4:c.756G>T , LRG_483t1:c.756G>T | NP_787110.2:p.Leu252= | |
| NM_178849.2:c.822G>T | NP_849180.1:p.Leu274= | |
| NM_178850.2:c.822G>T | NP_849181.1:p.Leu274= | |
| XM_005260407.2:c.939G>T | XP_005260464.1:p.Leu313= | |
| XM_011528797.1:c.870G>T | XP_011527099.1:p.Leu290= | |
| XM_011528798.1:c.870G>T | XP_011527100.1:p.Leu290= | |
| XM_005260407.4:c.939G>T | XP_005260464.1:p.Leu313= | |
| NM_001030003.3:c.756G>T | NP_001025174.1:p.Leu252= | |
| NM_001030004.3:c.756G>T | NP_001025175.1:p.Leu252= | |
| NM_001258355.2:c.801G>T | NP_001245284.1:p.Leu267= | |
| NM_001287182.2:c.747G>T | NP_001274111.1:p.Leu249= | |
| NM_001287184.2:c.747G>T | NP_001274113.1:p.Leu249= | |
| NM_178849.3:c.822G>T | NP_849180.1:p.Leu274= | |
| NM_178850.3:c.822G>T | NP_849181.1:p.Leu274= | |
| NM_000457.5:c.822G>T | NP_000448.3:p.Leu274= | |
| NM_000457.6:c.822G>T | NP_000448.3:p.Leu274= | |
| NM_001287183.2:c.747G>T | NP_001274112.1:p.Leu249= | |
| NM_175914.5:c.756G>T MANE Select | NP_787110.2:p.Leu252= |