Linked Data
dbSNP Id:
rs778084613
ExAC:
17:39768808 T / C
gnomAD v2:
17-39768808-T-C
gnomAD v3:
17-41612556-T-C
gnomAD v4:
17-41612556-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612556T>C , CM000679.2:g.41612556T>C | GRCh38 |
| NC_000017.10:g.39768808T>C , CM000679.1:g.39768808T>C | GRCh37 |
| NC_000017.9:g.37022334T>C | NCBI36 |
| NG_008301.1:g.5272A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.133A>G MANE Select | ENSP00000301653.3:p.Thr45Ala | |
| ENST00000301653.8:c.133A>G | ENSP00000301653.3:p.Thr45Ala | |
| ENST00000588319.1:n.210A>G | ||
| ENST00000590990.1:c.133A>G | ENSP00000467105.1:p.Thr45Ala | |
| ENST00000593067.1:c.-313+234A>G | ENSP00000467124.1:n.-313+234A>G | |
| NM_005557.3:c.133A>G | NP_005548.2:p.Thr45Ala | |
| NM_005557.4:c.133A>G MANE Select | NP_005548.2:p.Thr45Ala |