Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67939981C>A , CM000678.2:g.67939981C>A | GRCh38 |
| NC_000016.9:g.67973884C>A , CM000678.1:g.67973884C>A | GRCh37 |
| NC_000016.8:g.66531385C>A | NCBI36 |
| NG_009778.1:g.9132G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.1246G>T MANE Select | ENSP00000264005.5:p.Ala416Ser | |
| ENST00000264005.9:c.1246G>T | ENSP00000264005.5:p.Ala416Ser | |
| ENST00000570369.5:c.249G>T | ||
| ENST00000573538.5:c.984G>T | ENSP00000463220.1:n.984G>T | |
| NM_000229.1:c.1246G>T | NP_000220.1:p.Ala416Ser | |
| NM_000229.2:c.1246G>T MANE Select | NP_000220.1:p.Ala416Ser |