Linked Data
MyVariant Identifiers:
chr14:g.74726466C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74259763C>T , CM000676.2:g.74259763C>T | GRCh38 |
| NC_000014.8:g.74726466C>T , CM000676.1:g.74726466C>T | GRCh37 |
| NC_000014.7:g.73796219C>T | NCBI36 |
| NG_013092.1:g.25292C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261980.3:c.741C>T MANE Select | ENSP00000261980.2:p.Ser247= | |
| ENST00000261980.2:c.741C>T | ENSP00000261980.2:p.Ser247= | |
| NM_182894.2:c.741C>T | NP_878314.1:p.Ser247= | |
| XM_011536719.1:c.741C>T | XP_011535021.1:p.Ser247= | |
| NM_182894.3:c.741C>T MANE Select | NP_878314.1:p.Ser247= |