Linked Data
MyVariant Identifiers:
chr17:g.45822114C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47744748C>T , CM000679.2:g.47744748C>T | GRCh38 |
| NC_000017.10:g.45822114C>T , CM000679.1:g.45822114C>T | GRCh37 |
| NC_000017.9:g.43177113C>T | NCBI36 |
| NG_012166.1:g.16505C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000177694.2:c.990C>T MANE Select | ENSP00000177694.1:p.Ser330= | |
| ENST00000177694.1:c.990C>T | ENSP00000177694.1:p.Ser330= | |
| NM_013351.1:c.990C>T | NP_037483.1:p.Ser330= | |
| XM_011524698.1:c.1053C>T | XP_011523000.1:p.Ser351= | |
| XM_011524699.1:c.657C>T | XP_011523001.1:p.Ser219= | |
| NM_013351.2:c.990C>T MANE Select | NP_037483.1:p.Ser330= |