Linked Data
dbSNP Id:
rs2146049241
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.43551679A>G , CM000681.2:g.43551679A>G | GRCh38 |
| NC_000019.9:g.44055831A>G , CM000681.1:g.44055831A>G | GRCh37 |
| NC_000019.8:g.48747671A>G | NCBI36 |
| NG_033799.1:g.28900T>C , LRG_784:g.28900T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262887.10:c.1091T>C MANE Select | ENSP00000262887.5:p.Phe364Ser | |
| ENST00000262887.9:c.1091T>C | ENSP00000262887.4:p.Phe364Ser | |
| ENST00000543982.5:c.998T>C | ENSP00000443671.1:p.Phe333Ser | |
| ENST00000597811.5:c.701T>C | ||
| NM_006297.2:c.1091T>C , LRG_784t1:c.1091T>C | NP_006288.2:p.Phe364Ser | |
| NM_006297.3:c.1091T>C MANE Select | NP_006288.2:p.Phe364Ser |