Linked Data
dbSNP Id:
rs768033680
ExAC:
13:28498445 C / T
gnomAD v2:
13-28498445-C-T
gnomAD v4:
13-27924308-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924308C>T , CM000675.2:g.27924308C>T | GRCh38 |
| NC_000013.10:g.28498445C>T , CM000675.1:g.28498445C>T | GRCh37 |
| NC_000013.9:g.27396445C>T | NCBI36 |
| NG_008183.1:g.9278C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.459C>T MANE Select | ENSP00000370421.4:p.Tyr153= | |
| ENST00000381033.4:c.459C>T | ENSP00000370421.4:p.Tyr153= | |
| NM_000209.3:c.459C>T | NP_000200.1:p.Tyr153= | |
| XR_941579.1:n.2185C>T | ||
| XR_941580.1:n.1101C>T | ||
| XR_941580.2:n.1113C>T | ||
| NM_000209.4:c.459C>T MANE Select | NP_000200.1:p.Tyr153= |