Linked Data
ClinVar Variation Id:
236513
dbSNP Id:
rs147593839
ExAC:
16:57965773 G / A
gnomAD v2:
16-57965773-G-A
gnomAD v3:
16-57931869-G-A
gnomAD v4:
16-57931869-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.57931869G>A , CM000678.2:g.57931869G>A | GRCh38 |
| NC_000016.9:g.57965773G>A , CM000678.1:g.57965773G>A | GRCh37 |
| NC_000016.8:g.56523274G>A | NCBI36 |
| NG_016351.1:g.44248C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251102.13:c.1382C>T MANE Select | ENSP00000251102.8:p.Thr461Met | |
| ENST00000251102.12:c.1382C>T | ENSP00000251102.8:p.Thr461Met | |
| ENST00000564448.5:c.1364C>T | ENSP00000454633.1:p.Thr455Met | |
| ENST00000564450.1:n.120+7561C>T | ||
| ENST00000564654.1:n.771C>T | ||
| NM_001286130.1:c.1364C>T | NP_001273059.1:p.Thr455Met | |
| NM_001297.4:c.1382C>T | NP_001288.3:p.Thr461Met | |
| XM_006721134.2:c.1382C>T | XP_006721197.1:p.Thr461Met | |
| XM_011522870.1:c.233C>T | XP_011521172.1:p.Thr78Met | |
| XM_011522870.2:c.233C>T | XP_011521172.1:p.Thr78Met | |
| NM_001286130.2:c.1364C>T | NP_001273059.1:p.Thr455Met | |
| NM_001297.5:c.1382C>T MANE Select | NP_001288.3:p.Thr461Met |