Linked Data
dbSNP Id:
rs1569897293
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58782541T>G , CM000663.2:g.58782541T>G | GRCh38 |
| NC_000001.10:g.59248213T>G , CM000663.1:g.59248213T>G | GRCh37 |
| NC_000001.9:g.59020801T>G | NCBI36 |
| NG_047027.1:g.6573A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710273.1:c.596A>C | ENSP00000518166.1:p.Asn199Thr | |
| ENST00000371222.4:c.530A>C MANE Select | ENSP00000360266.2:p.Asn177Thr | |
| ENST00000678696.1:c.530A>C | ENSP00000503132.1:p.Asn177Thr | |
| ENST00000371222.3:c.530A>C | ENSP00000360266.2:p.Asn177Thr | |
| NM_002228.3:c.530A>C | NP_002219.1:p.Asn177Thr | |
| NM_002228.4:c.530A>C MANE Select | NP_002219.1:p.Asn177Thr |