Linked Data
MyVariant Identifiers:
chr16:g.67976765T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67942862T>A , CM000678.2:g.67942862T>A | GRCh38 |
| NC_000016.9:g.67976765T>A , CM000678.1:g.67976765T>A | GRCh37 |
| NC_000016.8:g.66534266T>A | NCBI36 |
| NG_009778.1:g.6251A>T | |
| NG_033098.1:g.30833A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.426A>T MANE Select | ENSP00000264005.5:p.Ala142= | |
| ENST00000264005.9:c.426A>T | ENSP00000264005.5:p.Ala142= | |
| ENST00000570369.5:c.154A>T | ||
| ENST00000570980.1:c.210A>T | ENSP00000464651.1:p.Ala70= | |
| ENST00000573538.5:c.69A>T | ENSP00000463220.1:p.Ala23= | |
| ENST00000573846.1:n.40A>T | ||
| ENST00000575277.1:n.204A>T | ||
| ENST00000575467.5:c.*121A>T | ENSP00000460653.1:n.*121A>T | |
| NM_000229.1:c.426A>T | NP_000220.1:p.Ala142= | |
| NM_000229.2:c.426A>T MANE Select | NP_000220.1:p.Ala142= |