Linked Data
ClinVar Variation Id:
403410
dbSNP Id:
rs118192159
ExAC:
19:39076588 C / T
gnomAD v2:
19-39076588-C-T
gnomAD v3:
19-38585948-C-T
gnomAD v4:
19-38585948-C-T
COSMIC:
COSM4467322
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38585948C>T , CM000681.2:g.38585948C>T | GRCh38 |
| NC_000019.9:g.39076588C>T , CM000681.1:g.39076588C>T | GRCh37 |
| NC_000019.8:g.43768428C>T | NCBI36 |
| NG_008866.1:g.157249C>T , LRG_766:g.157249C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000593677.2:c.1750C>T | ||
| ENST00000688602.1:c.3147C>T | ||
| ENST00000689936.1:c.3119C>T | ||
| ENST00000692547.1:n.207C>T | ||
| ENST00000359596.8:c.14814C>T MANE Select | ENSP00000352608.2:p.Ile4938= | |
| ENST00000355481.8:c.14799C>T | ENSP00000347667.3:p.Ile4933= | |
| ENST00000359596.7:c.14814C>T | ENSP00000352608.2:p.Ile4938= | |
| ENST00000360985.7:c.14796C>T | ENSP00000354254.4:p.Ile4932= | |
| NM_000540.2:c.14814C>T , LRG_766t1:c.14814C>T | NP_000531.2:p.Ile4938= | |
| NM_001042723.1:c.14799C>T | NP_001036188.1:p.Ile4933= | |
| XM_006723317.1:c.14796C>T | XP_006723380.1:p.Ile4932= | |
| XM_006723319.1:c.14781C>T | XP_006723382.1:p.Ile4927= | |
| XM_011527204.1:c.14811C>T | XP_011525506.1:p.Ile4937= | |
| XM_011527205.1:c.14727C>T | XP_011525507.1:p.Ile4909= | |
| XM_006723317.2:c.14796C>T | XP_006723380.1:p.Ile4932= | |
| XM_006723319.2:c.14781C>T | XP_006723382.1:p.Ile4927= | |
| XM_011527205.2:c.14727C>T | XP_011525507.1:p.Ile4909= | |
| NM_000540.3:c.14814C>T MANE Select | NP_000531.2:p.Ile4938= | |
| NM_001042723.2:c.14799C>T | NP_001036188.1:p.Ile4933= |