Linked Data
ClinVar Variation Id:
279848
ClinVar RCV Id:
RCV003155142
dbSNP Id:
rs74346519
ExAC:
16:3299759 G / A
gnomAD v2:
16-3299759-G-A
gnomAD v3:
16-3249759-G-A
gnomAD v4:
16-3249759-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3249759G>A , CM000678.2:g.3249759G>A | GRCh38 |
| NC_000016.9:g.3299759G>A , CM000678.1:g.3299759G>A | GRCh37 |
| NC_000016.8:g.3239760G>A | NCBI36 |
| NG_007871.1:g.11869C>T , LRG_190:g.11869C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000219596.6:c.932C>T MANE Select | ENSP00000219596.1:p.Ala311Val | |
| ENST00000219596.5:c.932C>T | ENSP00000219596.1:p.Ala311Val | |
| ENST00000339854.8:c.392C>T | ENSP00000339639.4:p.Ala131Val | |
| ENST00000536379.5:c.299C>T | ENSP00000445079.1:p.Ala100Val | |
| ENST00000536980.5:c.299C>T | ENSP00000444178.1:p.Ala100Val | |
| ENST00000537682.5:c.932C>T | ENSP00000438611.1:p.Ala311Val | |
| ENST00000538326.5:c.932C>T | ENSP00000437486.1:p.Ala311Val | |
| ENST00000539145.5:c.278-2513C>T | ENSP00000444471.1:n.278-2513C>T | |
| ENST00000541159.5:c.299C>T | ENSP00000438711.1:p.Ala100Val | |
| ENST00000542898.5:c.1025C>T | ENSP00000444615.1:p.Ala342Val | |
| ENST00000570511.5:c.911-2513C>T | ENSP00000458312.1:n.911-2513C>T | |
| ENST00000572244.5:c.278-3212C>T | ENSP00000461186.1:n.278-3212C>T | |
| ENST00000574583.5:c.278-2513C>T | ENSP00000460269.1:n.278-2513C>T | |
| ENST00000576315.5:c.278-2513C>T | ENSP00000460551.1:n.278-2513C>T | |
| ENST00000621655.1:c.299C>T | ENSP00000481436.1:p.Ala100Val | |
| NM_000243.2:c.932C>T , LRG_190t1:c.932C>T | NP_000234.1:p.Ala311Val | |
| NM_001198536.1:c.299C>T | NP_001185465.1:p.Ala100Val | |
| XM_017023236.2:c.932C>T | XP_016878725.1:p.Ala311Val | |
| XR_001751903.1:n.1121C>T | ||
| NM_000243.3:c.932C>T MANE Select | NP_000234.1:p.Ala311Val | |
| NM_001198536.2:c.299C>T | NP_001185465.2:p.Ala100Val |