Linked Data
ClinVar Variation Id:
288970
dbSNP Id:
rs565563742
ExAC:
19:47258761 T / A
gnomAD v2:
19-47258761-T-A
gnomAD v3:
19-46755504-T-A
gnomAD v4:
19-46755504-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.46755504T>A , CM000681.2:g.46755504T>A | GRCh38 |
| NC_000019.9:g.47258761T>A , CM000681.1:g.47258761T>A | GRCh37 |
| NC_000019.8:g.51950601T>A | NCBI36 |
| NG_008898.2:g.14459T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318584.10:c.54T>A MANE Select | ENSP00000326570.4:p.Leu18= | |
| ENST00000318584.9:c.54T>A | ENSP00000326570.4:p.Leu18= | |
| ENST00000391909.7:c.54T>A | ENSP00000375776.2:p.Leu18= | |
| ENST00000593800.5:c.54T>A | ENSP00000471209.1:p.Leu18= | |
| ENST00000593875.5:c.54T>A | ENSP00000470297.1:p.Leu18= | |
| ENST00000593902.1:c.54T>A | ENSP00000470901.1:p.Leu18= | |
| ENST00000594467.5:c.-345-31T>A | ENSP00000471971.1:n.-345-31T>A | |
| ENST00000595570.5:c.54T>A | ENSP00000470929.1:p.Leu18= | |
| ENST00000595868.5:c.54T>A | ENSP00000471573.1:p.Leu18= | |
| ENST00000596460.5:c.54T>A | ENSP00000469373.1:p.Leu18= | |
| ENST00000596974.5:n.311-31T>A | ||
| ENST00000597313.5:c.54T>A | ENSP00000472370.1:p.Leu18= | |
| ENST00000597339.5:n.247-6329T>A | ||
| ENST00000598271.5:c.54T>A | ENSP00000471088.1:p.Leu18= | |
| ENST00000600005.5:c.54T>A | ENSP00000470335.1:p.Leu18= | |
| ENST00000600227.5:c.54T>A | ENSP00000468825.1:p.Leu18= | |
| ENST00000600629.5:c.54T>A | ENSP00000470096.1:p.Leu18= | |
| ENST00000600646.5:n.247+6839T>A | ||
| ENST00000600834.5:c.54T>A | ENSP00000470024.1:p.Leu18= | |
| ENST00000601299.5:c.54T>A | ENSP00000470103.1:p.Leu18= | |
| ENST00000602181.5:c.54T>A | ENSP00000472981.1:p.Leu18= | |
| ENST00000602250.5:c.54T>A | ENSP00000472807.1:p.Leu18= | |
| NM_001039885.2:c.54T>A | NP_001034974.1:p.Leu18= | |
| NM_024301.4:c.54T>A | NP_077277.1:p.Leu18= | |
| XM_005259247.1:c.54T>A | XP_005259304.1:p.Leu18= | |
| XM_005259248.1:c.54T>A | XP_005259305.1:p.Leu18= | |
| XM_005259249.3:c.54T>A | XP_005259306.1:p.Leu18= | |
| XM_005259250.3:c.54T>A | XP_005259307.1:p.Leu18= | |
| XM_011527301.1:c.54T>A | XP_011525603.1:p.Leu18= | |
| XM_011527302.1:c.54T>A | XP_011525604.1:p.Leu18= | |
| XM_011527303.1:c.54T>A | XP_011525605.1:p.Leu18= | |
| XM_011527304.1:c.54T>A | XP_011525606.1:p.Leu18= | |
| XM_011527305.1:c.54T>A | XP_011525607.1:p.Leu18= | |
| XM_011527306.1:c.54T>A | XP_011525608.1:p.Leu18= | |
| XM_011527307.1:c.54T>A | XP_011525609.1:p.Leu18= | |
| XM_005259247.2:c.54T>A | XP_005259304.1:p.Leu18= | |
| XM_005259248.2:c.54T>A | XP_005259305.1:p.Leu18= | |
| XM_005259249.4:c.54T>A | XP_005259306.1:p.Leu18= | |
| XM_011527306.2:c.54T>A | XP_011525608.1:p.Leu18= | |
| XM_017027297.2:c.54T>A | XP_016882786.1:p.Leu18= | |
| XM_024451707.1:c.54T>A | XP_024307475.1:p.Leu18= | |
| NM_001039885.3:c.54T>A | NP_001034974.1:p.Leu18= | |
| NM_024301.5:c.54T>A MANE Select | NP_077277.1:p.Leu18= |