Linked Data
dbSNP Id:
rs949211195
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56041937G>T , CM000674.2:g.56041937G>T | GRCh38 |
| NC_000012.11:g.56435721G>T , CM000674.1:g.56435721G>T | GRCh37 |
| NC_000012.10:g.54721988G>T | NCBI36 |
| NG_023201.1:g.5036G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356464.10:c.-230G>T | ENSP00000348849.5:n.-230G>T | |
| ENST00000646449.2:c.-230G>T MANE Select | ENSP00000496643.1:n.-230G>T | |
| ENST00000356464.9:c.-230G>T | ENSP00000348849.5:n.-230G>T | |
| ENST00000552361.1:c.-162G>T | ENSP00000450339.1:n.-162G>T | |
| NM_001029.3:c.-230G>T | NP_001020.2:n.-230G>T | |
| NM_001029.5:c.-230G>T MANE Select | NP_001020.2:n.-230G>T | |
| XR_944989.3:n.67C>A | ||
| XR_944990.3:n.67C>A |