Linked Data
MyVariant Identifiers:
chr16:g.28856788T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28845467T>G , CM000678.2:g.28845467T>G | GRCh38 |
| NC_000016.9:g.28856788T>G , CM000678.1:g.28856788T>G | GRCh37 |
| NC_000016.8:g.28764289T>G | NCBI36 |
| NG_008964.1:g.5942A>C | |
| NG_029706.2:g.3868T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313511.8:c.261A>C MANE Select | ENSP00000322439.3:p.Gly87= | |
| ENST00000313511.7:c.261A>C | ENSP00000322439.3:p.Gly87= | |
| ENST00000565012.1:c.248-412A>C | ENSP00000455007.1:n.248-412A>C | |
| NM_003321.4:c.261A>C | NP_003312.3:p.Gly87= | |
| XM_011545928.1:c.261A>C | XP_011544230.1:p.Gly87= | |
| NM_001365360.1:c.261A>C | NP_001352289.1:p.Gly87= | |
| NM_003321.5:c.261A>C MANE Select | NP_003312.3:p.Gly87= | |
| NM_001365360.2:c.261A>C | NP_001352289.1:p.Gly87= |