Linked Data
MyVariant Identifiers:
chr17:g.45363689G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47286323G>T , CM000679.2:g.47286323G>T | GRCh38 |
| NC_000017.10:g.45363689G>T , CM000679.1:g.45363689G>T | GRCh37 |
| NC_000017.9:g.42718688G>T | NCBI36 |
| NG_008332.2:g.37482G>T , LRG_481:g.37482G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.678G>T | ENSP00000513002.1:p.Val226= | |
| ENST00000559488.7:c.678G>T MANE Select | ENSP00000452786.2:p.Val226= | |
| ENST00000559488.5:c.678G>T | ENSP00000452786.1:p.Val226= | |
| ENST00000560629.1:c.643G>T | ||
| ENST00000571680.1:c.678G>T | ENSP00000461626.1:p.Val226= | |
| NM_000212.2:c.678G>T , LRG_481t1:c.678G>T | NP_000203.2:p.Val226= | |
| NM_000212.3:c.678G>T MANE Select | NP_000203.2:p.Val226= |