Linked Data
MyVariant Identifiers:
chr14:g.24728333T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.24259127T>G , CM000676.2:g.24259127T>G | GRCh38 |
| NC_000014.8:g.24728333T>G , CM000676.1:g.24728333T>G | GRCh37 |
| NC_000014.7:g.23798173T>G | NCBI36 |
| NG_007150.1:g.9040A>C | |
| NG_007150.2:g.9040A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000206765.11:c.1107A>C MANE Select | ENSP00000206765.6:p.Gly369= | |
| ENST00000206765.10:c.1107A>C | ENSP00000206765.6:p.Gly369= | |
| ENST00000544573.5:c.-28-739A>C | ENSP00000439446.1:n.-28-739A>C | |
| ENST00000559136.1:c.180A>C | ENSP00000453337.1:p.Gly60= | |
| NM_000359.2:c.1107A>C | NP_000350.1:p.Gly369= | |
| NM_000359.3:c.1107A>C MANE Select | NP_000350.1:p.Gly369= |