Linked Data
ClinVar Variation Id:
2414425
ClinVar RCV Id:
RCV003106758
dbSNP Id:
rs104895083
ExAC:
16:3297166 G / T
gnomAD v2:
16-3297166-G-T
gnomAD v3:
16-3247166-G-T
gnomAD v4:
16-3247166-G-T
COSMIC:
COSM282758
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3247166G>T , CM000678.2:g.3247166G>T | GRCh38 |
| NC_000016.9:g.3297166G>T , CM000678.1:g.3297166G>T | GRCh37 |
| NC_000016.8:g.3237167G>T | NCBI36 |
| NG_007871.1:g.14462C>A , LRG_190:g.14462C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219596.6:c.1437C>A MANE Select | ENSP00000219596.1:p.Phe479Leu | |
| ENST00000219596.5:c.1437C>A | ENSP00000219596.1:p.Phe479Leu | |
| ENST00000339854.8:c.897C>A | ENSP00000339639.4:p.Phe299Leu | |
| ENST00000536379.5:c.804C>A | ENSP00000445079.1:p.Phe268Leu | |
| ENST00000536980.5:c.804C>A | ENSP00000444178.1:p.Phe268Leu | |
| ENST00000537682.5:c.1437C>A | ENSP00000438611.1:p.Phe479Leu | |
| ENST00000538326.5:c.*62C>A | ENSP00000437486.1:n.*62C>A | |
| ENST00000539145.5:c.358C>A | ENSP00000444471.1:n.358C>A | |
| ENST00000539154.1:n.802C>A | ||
| ENST00000541159.5:c.804C>A | ENSP00000438711.1:p.Phe268Leu | |
| ENST00000542898.5:c.1530C>A | ENSP00000444615.1:p.Phe510Leu | |
| ENST00000570511.5:c.991C>A | ENSP00000458312.1:n.991C>A | |
| ENST00000572244.5:c.278-619C>A | ENSP00000461186.1:n.278-619C>A | |
| ENST00000574583.5:c.358C>A | ENSP00000460269.1:n.358C>A | |
| ENST00000576315.5:c.358C>A | ENSP00000460551.1:n.358C>A | |
| ENST00000621655.1:c.804C>A | ENSP00000481436.1:p.Phe268Leu | |
| NM_000243.2:c.1437C>A , LRG_190t1:c.1437C>A | NP_000234.1:p.Phe479Leu | |
| NM_001198536.1:c.804C>A | NP_001185465.1:p.Phe268Leu | |
| XM_017023236.2:c.1434C>A | XP_016878725.1:p.Phe478Leu | |
| XR_001751903.1:n.1626C>A | ||
| NM_000243.3:c.1437C>A MANE Select | NP_000234.1:p.Phe479Leu | |
| NM_001198536.2:c.804C>A | NP_001185465.2:p.Phe268Leu |