Linked Data
MyVariant Identifiers:
chr16:g.28856338G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28845017G>T , CM000678.2:g.28845017G>T | GRCh38 |
| NC_000016.9:g.28856338G>T , CM000678.1:g.28856338G>T | GRCh37 |
| NC_000016.8:g.28763839G>T | NCBI36 |
| NG_008964.1:g.6392C>A | |
| NG_029706.2:g.3418G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313511.8:c.453C>A MANE Select | ENSP00000322439.3:p.Ile151= | |
| ENST00000313511.7:c.453C>A | ENSP00000322439.3:p.Ile151= | |
| ENST00000565012.1:c.286C>A | ENSP00000455007.1:p.Pro96Thr | |
| NM_003321.4:c.453C>A | NP_003312.3:p.Ile151= | |
| XM_011545928.1:c.453C>A | XP_011544230.1:p.Ile151= | |
| NM_001365360.1:c.453C>A | NP_001352289.1:p.Ile151= | |
| NM_003321.5:c.453C>A MANE Select | NP_003312.3:p.Ile151= | |
| NM_001365360.2:c.453C>A | NP_001352289.1:p.Ile151= |