Linked Data
MyVariant Identifiers:
chr14:g.75475789A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75009086A>T , CM000676.2:g.75009086A>T | GRCh38 |
| NC_000014.8:g.75475789A>T , CM000676.1:g.75475789A>T | GRCh37 |
| NC_000014.7:g.74545542A>T | NCBI36 |
| NG_013333.1:g.11178A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266126.10:c.954A>T MANE Select | ENSP00000266126.5:p.Pro318= | |
| ENST00000266126.9:c.954A>T | ENSP00000266126.5:p.Pro318= | |
| ENST00000556668.1:n.534A>T | ||
| NM_014239.3:c.954A>T | NP_055054.1:p.Pro318= | |
| NM_014239.4:c.954A>T MANE Select | NP_055054.1:p.Pro318= |