Linked Data
ClinVar Variation Id:
329142
dbSNP Id:
rs188314477
gnomAD v2:
19-39078195-C-T
gnomAD v3:
19-38587555-C-T
gnomAD v4:
19-38587555-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38587555C>T , CM000681.2:g.38587555C>T | GRCh38 |
| NC_000019.9:g.39078195C>T , CM000681.1:g.39078195C>T | GRCh37 |
| NC_000019.8:g.43770035C>T | NCBI36 |
| NG_008866.1:g.158856C>T , LRG_766:g.158856C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.1957+979C>T | ||
| ENST00000688602.1:c.3585C>T | ||
| ENST00000692547.1:n.645C>T | ||
| ENST00000359596.8:c.*135C>T MANE Select | ENSP00000352608.2:n.*135C>T | |
| ENST00000355481.8:c.*135C>T | ENSP00000347667.3:n.*135C>T | |
| ENST00000360985.7:c.*135C>T | ENSP00000354254.4:n.*135C>T | |
| NM_000540.2:c.*135C>T , LRG_766t1:c.*135C>T | NP_000531.2:n.*135C>T | |
| NM_001042723.1:c.*135C>T | NP_001036188.1:n.*135C>T | |
| XM_006723317.1:c.*135C>T | XP_006723380.1:n.*135C>T | |
| XM_006723319.1:c.*135C>T | XP_006723382.1:n.*135C>T | |
| XM_011527204.1:c.*135C>T | XP_011525506.1:n.*135C>T | |
| XM_011527205.1:c.*135C>T | XP_011525507.1:n.*135C>T | |
| XM_006723317.2:c.*135C>T | XP_006723380.1:n.*135C>T | |
| XM_006723319.2:c.*135C>T | XP_006723382.1:n.*135C>T | |
| XM_011527205.2:c.*135C>T | XP_011525507.1:n.*135C>T | |
| NM_000540.3:c.*135C>T MANE Select | NP_000531.2:n.*135C>T | |
| NM_001042723.2:c.*135C>T | NP_001036188.1:n.*135C>T |