Linked Data
MyVariant Identifiers:
chr16:g.89986113A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89919705A>T , CM000678.2:g.89919705A>T | GRCh38 |
| NC_000016.9:g.89986113A>T , CM000678.1:g.89986113A>T | GRCh37 |
| NC_000016.8:g.88513614A>T | NCBI36 |
| NG_012026.1:g.6827A>T | |
| NG_027810.1:g.2697A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555147.2:c.447A>T MANE Select | ENSP00000451605.1:p.Ala149= | |
| ENST00000639847.1:c.447A>T | ENSP00000492011.1:p.Ala149= | |
| ENST00000555147.1:c.447A>T | ENSP00000451605.1:p.Ala149= | |
| ENST00000555427.1:c.447A>T | ENSP00000451760.1:p.Ala149= | |
| ENST00000556922.1:c.447A>T | ENSP00000451560.1:p.Ala149= | |
| NM_002386.3:c.447A>T | NP_002377.4:p.Ala149= | |
| NM_002386.4:c.447A>T MANE Select | NP_002377.4:p.Ala149= |