Linked Data
dbSNP Id:
rs776890182
ExAC:
16:2328456 A / T
gnomAD v2:
16-2328456-A-T
gnomAD v4:
16-2278455-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2278455A>T , CM000678.2:g.2278455A>T | GRCh38 |
| NC_000016.9:g.2328456A>T , CM000678.1:g.2328456A>T | GRCh37 |
| NC_000016.8:g.2268457A>T | NCBI36 |
| NG_011790.1:g.67292T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301732.10:c.4551T>A MANE Select | ENSP00000301732.5:p.Gly1517= | |
| ENST00000301732.9:c.4551T>A | ENSP00000301732.5:p.Gly1517= | |
| ENST00000382381.7:c.4377T>A | ENSP00000371818.3:p.Gly1459= | |
| ENST00000566200.1:n.1072T>A | ||
| NM_001089.2:c.4551T>A | NP_001080.2:p.Gly1517= | |
| NM_001089.3:c.4551T>A MANE Select | NP_001080.2:p.Gly1517= |