Linked Data
MyVariant Identifiers:
chr16:g.28856743C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28845422C>A , CM000678.2:g.28845422C>A | GRCh38 |
| NC_000016.9:g.28856743C>A , CM000678.1:g.28856743C>A | GRCh37 |
| NC_000016.8:g.28764244C>A | NCBI36 |
| NG_008964.1:g.5987G>T | |
| NG_029706.2:g.3823C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313511.8:c.306G>T MANE Select | ENSP00000322439.3:p.Pro102= | |
| ENST00000313511.7:c.306G>T | ENSP00000322439.3:p.Pro102= | |
| ENST00000565012.1:c.248-367G>T | ENSP00000455007.1:n.248-367G>T | |
| NM_003321.4:c.306G>T | NP_003312.3:p.Pro102= | |
| XM_011545928.1:c.306G>T | XP_011544230.1:p.Pro102= | |
| NM_001365360.1:c.306G>T | NP_001352289.1:p.Pro102= | |
| NM_003321.5:c.306G>T MANE Select | NP_003312.3:p.Pro102= | |
| NM_001365360.2:c.306G>T | NP_001352289.1:p.Pro102= |