Linked Data
MyVariant Identifiers:
chr16:g.2036005C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1986004C>A , CM000678.2:g.1986004C>A | GRCh38 |
| NC_000016.9:g.2036005C>A , CM000678.1:g.2036005C>A | GRCh37 |
| NC_000016.8:g.1976006C>A | NCBI36 |
| NG_016288.1:g.6856C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.369C>A | ENSP00000455885.1:p.Gly123= | |
| ENST00000248114.7:c.594C>A MANE Select | ENSP00000248114.6:p.Gly198= | |
| ENST00000248114.6:c.594C>A | ENSP00000248114.6:p.Gly198= | |
| ENST00000565658.1:n.751C>A | ||
| ENST00000567719.1:c.369C>A | ENSP00000455885.1:p.Gly123= | |
| ENST00000569451.1:c.*67C>A | ENSP00000456432.1:n.*67C>A | |
| NM_005262.2:c.594C>A | NP_005253.3:p.Gly198= | |
| NM_005262.3:c.594C>A MANE Select | NP_005253.3:p.Gly198= |