Linked Data
ClinVar Variation Id:
1560558
ClinVar RCV Id:
RCV002209186
dbSNP Id:
rs528199992
gnomAD v3:
14-74480714-G-T
gnomAD v4:
14-74480714-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74480714G>T , CM000676.2:g.74480714G>T | GRCh38 |
| NC_000014.8:g.74947417G>T , CM000676.1:g.74947417G>T | GRCh37 |
| NC_000014.7:g.74017170G>T | NCBI36 |
| NG_007117.1:g.17668C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000555619.6:c.429C>A MANE Select | ENSP00000451112.2:p.Ile143= | |
| ENST00000238633.6:c.429C>A | ENSP00000238633.2:p.Ile143= | |
| ENST00000434013.6:c.429C>A | ENSP00000412103.2:p.Ile143= | |
| ENST00000541064.5:c.364-426C>A | ENSP00000442488.1:n.364-426C>A | |
| ENST00000553490.5:c.429C>A | ENSP00000451180.1:p.Ile143= | |
| ENST00000554482.1:c.224C>A | ENSP00000451314.1:n.224C>A | |
| ENST00000555619.5:c.429C>A | ENSP00000451112.1:p.Ile143= | |
| ENST00000556009.5:c.494C>A | ||
| ENST00000557510.5:c.429C>A | ENSP00000451206.1:p.Ile143= | |
| NM_006432.3:c.429C>A | NP_006423.1:p.Ile143= | |
| NM_001363688.1:c.429C>A | NP_001350617.1:p.Ile143= | |
| NM_006432.4:c.429C>A | NP_006423.1:p.Ile143= | |
| NM_001375440.1:c.364-426C>A | NP_001362369.1:n.364-426C>A | |
| NM_006432.5:c.429C>A MANE Select | NP_006423.1:p.Ile143= |