Linked Data
MyVariant Identifiers:
chr14:g.31863265T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.31394059T>G , CM000676.2:g.31394059T>G | GRCh38 |
| NC_000014.8:g.31863265T>G , CM000676.1:g.31863265T>G | GRCh37 |
| NC_000014.7:g.30933016T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000543095.7:c.765A>C MANE Select | ENSP00000437968.2:p.Pro255= | |
| ENST00000543095.6:c.765A>C | ENSP00000437968.2:p.Pro255= | |
| ENST00000549185.5:c.*861A>C | ENSP00000446654.1:n.*861A>C | |
| NM_015473.3:c.765A>C | NP_056288.2:p.Pro255= | |
| NM_015473.4:c.765A>C MANE Select | NP_056288.2:p.Pro255= |