Linked Data
dbSNP Id:
rs1580653544
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135445308A>C , CM000667.2:g.135445308A>C | GRCh38 |
| NC_000005.9:g.134780998A>C , CM000667.1:g.134780998A>C | GRCh37 |
| NC_000005.8:g.134808897A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000537858.2:c.*4146T>G (TIFAB) MANE Select | ENSP00000440509.1:n.*4146T>G | |
| ENST00000503143.3:c.*1066T>G (DCANP1) MANE Select | ENSP00000421871.1:n.*1066T>G | |
| ENST00000537858.1:c.*4146T>G (TIFAB) | ENSP00000440509.1:n.*4146T>G | |
| NM_130848.2:c.*1066T>G (DCANP1) | NP_570900.1:n.*1066T>G | |
| NM_001099221.2:c.*4146T>G (TIFAB) MANE Select | NP_001092691.1:n.*4146T>G | |
| NM_130848.3:c.*1066T>G (DCANP1) MANE Select | NP_570900.1:n.*1066T>G |