Linked Data
dbSNP Id:
rs370920743
ExAC:
19:49207138 T / C
gnomAD v3:
19-48703881-T-C
gnomAD v4:
19-48703881-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48703881T>C , CM000681.2:g.48703881T>C | GRCh38 |
| NC_000019.9:g.49207138T>C , CM000681.1:g.49207138T>C | GRCh37 |
| NC_000019.8:g.53898950T>C | NCBI36 |
| NG_007511.1:g.12911T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000425340.3:c.925T>C MANE Select | ENSP00000387498.2:p.Tyr309His | |
| ENST00000522966.2:c.925T>C | ENSP00000430227.2:p.Tyr309His | |
| ENST00000391876.5:c.925T>C | ENSP00000375748.4:p.Tyr309His | |
| ENST00000425340.2:c.925T>C | ENSP00000387498.2:p.Tyr309His | |
| NM_000511.5:c.925T>C | NP_000502.4:p.Tyr309His | |
| NM_001097638.2:c.925T>C | NP_001091107.1:p.Tyr309His | |
| NM_000511.6:c.925T>C MANE Select | NP_000502.4:p.Tyr309His | |
| NM_001097638.3:c.925T>C | NP_001091107.1:p.Tyr309His |