Linked Data
ClinVar Variation Id:
464021
dbSNP Id:
rs578056399
ExAC:
5:156186295 C / T
gnomAD v2:
5-156186295-C-T
gnomAD v3:
5-156759284-C-T
gnomAD v4:
5-156759284-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.156759284C>T , CM000667.2:g.156759284C>T | GRCh38 |
| NC_000005.9:g.156186295C>T , CM000667.1:g.156186295C>T | GRCh37 |
| NC_000005.8:g.156118873C>T | NCBI36 |
| NG_008693.2:g.893942C>T , LRG_205:g.893942C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337851.9:c.767C>T MANE Select | ENSP00000338343.4:p.Thr256Met | |
| ENST00000337851.8:c.767C>T | ENSP00000338343.4:p.Thr256Met | |
| ENST00000435422.7:c.764C>T | ENSP00000403003.2:p.Thr255Met | |
| NM_000337.5:c.767C>T , LRG_205t1:c.767C>T | NP_000328.2:p.Thr256Met | |
| NM_001128209.1:c.764C>T | NP_001121681.1:p.Thr255Met | |
| XM_005265966.3:c.767C>T | XP_005266023.1:p.Thr256Met | |
| XM_006714911.2:c.767C>T | XP_006714974.1:p.Thr256Met | |
| XM_011534621.1:c.764C>T | XP_011532923.1:p.Thr255Met | |
| XM_005265966.5:c.767C>T | XP_005266023.1:p.Thr256Met | |
| XM_011534621.2:c.764C>T | XP_011532923.1:p.Thr255Met | |
| XM_017009723.2:c.767C>T | XP_016865212.1:p.Thr256Met | |
| XM_017009724.1:c.767C>T | XP_016865213.1:p.Thr256Met | |
| NM_001128209.2:c.764C>T | NP_001121681.1:p.Thr255Met | |
| NM_000337.6:c.767C>T MANE Select | NP_000328.2:p.Thr256Met |