Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.73682976C>T , CM000669.2:g.73682976C>T | GRCh38 |
| NC_000007.13:g.73097306C>T , CM000669.1:g.73097306C>T | GRCh37 |
| NC_000007.12:g.72735242C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395176.3:c.448G>A MANE Select | ENSP00000378605.1:p.Gly150Ser | |
| ENST00000395176.2:c.448G>A | ENSP00000378605.1:p.Gly150Ser | |
| NM_032317.2:c.448G>A | NP_115693.2:p.Gly150Ser | |
| NM_032317.3:c.448G>A MANE Select | NP_115693.2:p.Gly150Ser |