Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56983365G>T , CM000678.2:g.56983365G>T | GRCh38 |
| NC_000016.9:g.57017277G>T , CM000678.1:g.57017277G>T | GRCh37 |
| NC_000016.8:g.55574778G>T | NCBI36 |
| NG_008952.1:g.26443G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000200676.8:c.1361G>T MANE Select | ENSP00000200676.3:p.Gly454Val | |
| ENST00000650358.1:n.1759G>T | ||
| ENST00000200676.7:c.1361G>T | ENSP00000200676.3:p.Gly454Val | |
| ENST00000379780.6:c.1181G>T | ENSP00000369106.2:p.Gly394Val | |
| ENST00000566128.1:c.1166G>T | ENSP00000456276.1:p.Gly389Val | |
| NM_000078.2:c.1361G>T | NP_000069.2:p.Gly454Val | |
| NM_001286085.1:c.1181G>T | NP_001273014.1:p.Gly394Val | |
| NM_000078.3:c.1361G>T MANE Select | NP_000069.2:p.Gly454Val | |
| NM_001286085.2:c.1181G>T | NP_001273014.1:p.Gly394Val |