Linked Data
ClinVar Variation Id:
12946
dbSNP Id:
rs1047781
ExAC:
19:49206631 A / T
gnomAD v2:
19-49206631-A-T
gnomAD v3:
19-48703374-A-T
gnomAD v4:
19-48703374-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48703374A>T , CM000681.2:g.48703374A>T | GRCh38 |
| NC_000019.9:g.49206631A>T , CM000681.1:g.49206631A>T | GRCh37 |
| NC_000019.8:g.53898443A>T | NCBI36 |
| NG_007511.1:g.12404A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000425340.3:c.418A>T MANE Select | ENSP00000387498.2:p.Ile140Phe | |
| ENST00000522966.2:c.418A>T | ENSP00000430227.2:p.Ile140Phe | |
| ENST00000391876.5:c.418A>T | ENSP00000375748.4:p.Ile140Phe | |
| ENST00000425340.2:c.418A>T | ENSP00000387498.2:p.Ile140Phe | |
| ENST00000522966.1:c.418A>T | ENSP00000430227.1:p.Ile140Phe | |
| NM_000511.5:c.418A>T | NP_000502.4:p.Ile140Phe | |
| NM_001097638.2:c.418A>T | NP_001091107.1:p.Ile140Phe | |
| NR_131188.1:n.475T>A | ||
| NM_000511.6:c.418A>T MANE Select | NP_000502.4:p.Ile140Phe | |
| NM_001097638.3:c.418A>T | NP_001091107.1:p.Ile140Phe |