Linked Data
MyVariant Identifiers:
chr14:g.74726322T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74259619T>C , CM000676.2:g.74259619T>C | GRCh38 |
| NC_000014.8:g.74726322T>C , CM000676.1:g.74726322T>C | GRCh37 |
| NC_000014.7:g.73796075T>C | NCBI36 |
| NG_013092.1:g.25148T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261980.3:c.597T>C MANE Select | ENSP00000261980.2:p.Arg199= | |
| ENST00000261980.2:c.597T>C | ENSP00000261980.2:p.Arg199= | |
| NM_182894.2:c.597T>C | NP_878314.1:p.Arg199= | |
| XM_011536719.1:c.597T>C | XP_011535021.1:p.Arg199= | |
| NM_182894.3:c.597T>C MANE Select | NP_878314.1:p.Arg199= |