Linked Data
ClinVar Variation Id:
2402
dbSNP Id:
rs28941473
ExAC:
7:65551738 G / A
gnomAD v2:
7-65551738-G-A
gnomAD v3:
7-66086751-G-A
gnomAD v4:
7-66086751-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.66086751G>A , CM000669.2:g.66086751G>A | GRCh38 |
| NC_000007.13:g.65551738G>A , CM000669.1:g.65551738G>A | GRCh37 |
| NC_000007.12:g.65189173G>A | NCBI36 |
| NG_009288.1:g.15963G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000304874.14:c.532G>A MANE Select | ENSP00000307188.9:p.Val178Met | |
| ENST00000362000.10:c.337G>A | ENSP00000354710.6:p.Val113Met | |
| ENST00000380839.9:c.524+89G>A | ENSP00000370219.4:n.524+89G>A | |
| ENST00000395331.4:c.532G>A | ENSP00000378740.3:p.Val178Met | |
| ENST00000395332.8:c.532G>A | ENSP00000378741.3:p.Val178Met | |
| ENST00000671817.1:c.524+89G>A | ENSP00000500462.1:n.524+89G>A | |
| ENST00000672498.1:c.447-978G>A | ENSP00000500227.1:n.447-978G>A | |
| ENST00000672586.1:n.437G>A | ||
| ENST00000672676.1:n.702G>A | ||
| ENST00000673149.1:n.344G>A | ||
| ENST00000673350.1:n.780G>A | ||
| ENST00000673518.1:c.524+89G>A | ENSP00000499889.1:n.524+89G>A | |
| ENST00000673594.1:n.381G>A | ||
| ENST00000304874.13:c.532G>A | ENSP00000307188.9:p.Val178Met | |
| ENST00000362000.9:c.337G>A | ENSP00000354710.5:p.Val113Met | |
| ENST00000380839.8:c.524+89G>A | ENSP00000370219.4:n.524+89G>A | |
| ENST00000395331.3:c.532G>A | ENSP00000378740.3:p.Val178Met | |
| ENST00000395332.7:c.532G>A | ENSP00000378741.3:p.Val178Met | |
| ENST00000487982.5:n.598G>A | ||
| NM_000048.3:c.532G>A | NP_000039.2:p.Val178Met | |
| NM_001024943.1:c.532G>A | NP_001020114.1:p.Val178Met | |
| NM_001024944.1:c.532G>A | NP_001020115.1:p.Val178Met | |
| NM_001024946.1:c.524+89G>A | NP_001020117.1:n.524+89G>A | |
| NM_000048.4:c.532G>A MANE Select | NP_000039.2:p.Val178Met | |
| NM_001024943.2:c.532G>A | NP_001020114.1:p.Val178Met | |
| NM_001024944.2:c.532G>A | NP_001020115.1:p.Val178Met | |
| NM_001024946.2:c.524+89G>A | NP_001020117.1:n.524+89G>A |