Linked Data
MyVariant Identifiers:
chr16:g.67974284C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940381C>A , CM000678.2:g.67940381C>A | GRCh38 |
| NC_000016.9:g.67974284C>A , CM000678.1:g.67974284C>A | GRCh37 |
| NC_000016.8:g.66531785C>A | NCBI36 |
| NG_009778.1:g.8732G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.846G>T MANE Select | ENSP00000264005.5:p.Ala282= | |
| ENST00000264005.9:c.846G>T | ENSP00000264005.5:p.Ala282= | |
| ENST00000570369.5:c.156-307G>T | ||
| ENST00000570980.1:c.630G>T | ENSP00000464651.1:p.Ala210= | |
| ENST00000573538.5:c.584G>T | ENSP00000463220.1:n.584G>T | |
| NM_000229.1:c.846G>T | NP_000220.1:p.Ala282= | |
| NM_000229.2:c.846G>T MANE Select | NP_000220.1:p.Ala282= |