Linked Data
ClinVar Variation Id:
360556
ClinVar RCV Id:
RCV000385298
dbSNP Id:
rs886062404
gnomAD v4:
7-65982139-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.65982139C>T , CM000669.2:g.65982139C>T | GRCh38 |
| NC_000007.13:g.65447126C>T , CM000669.1:g.65447126C>T | GRCh37 |
| NC_000007.12:g.65084561C>T | NCBI36 |
| NG_016197.1:g.5176G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000304895.9:c.45G>A MANE Select | ENSP00000302728.4:p.Leu15= | |
| ENST00000304895.8:c.45G>A | ENSP00000302728.4:p.Leu15= | |
| ENST00000421103.5:c.45G>A | ENSP00000391390.1:p.Leu15= | |
| ENST00000430730.5:c.45G>A | ENSP00000411859.1:p.Leu15= | |
| ENST00000446111.1:c.45G>A | ENSP00000416793.1:p.Leu15= | |
| ENST00000447929.5:c.45G>A | ENSP00000411262.1:p.Leu15= | |
| NM_000181.3:c.45G>A | NP_000172.2:p.Leu15= | |
| NM_001284290.1:c.45G>A | NP_001271219.1:p.Leu15= | |
| NM_001293104.1:c.-341G>A | NP_001280033.1:n.-341G>A | |
| NM_001293105.1:c.-285G>A | NP_001280034.1:n.-285G>A | |
| NR_120531.1:n.176G>A | ||
| XM_005250297.3:c.45G>A | XP_005250354.1:p.Leu15= | |
| XM_011516113.1:c.-285G>A | XP_011514415.1:n.-285G>A | |
| XR_927461.1:n.171G>A | ||
| XM_005250297.4:c.45G>A | XP_005250354.1:p.Leu15= | |
| XM_011516114.2:c.-641G>A | XP_011514416.1:n.-641G>A | |
| XM_017012091.1:c.-285G>A | XP_016867580.1:n.-285G>A | |
| XM_017012092.1:c.-341G>A | XP_016867581.1:n.-341G>A | |
| XM_017012093.2:c.-641G>A | XP_016867582.1:n.-641G>A | |
| XR_001744658.2:n.90G>A | ||
| XR_001744659.2:n.90G>A | ||
| XR_001744660.2:n.90G>A | ||
| XR_001744661.2:n.90G>A | ||
| XR_927461.3:n.90G>A | ||
| NM_000181.4:c.45G>A MANE Select | NP_000172.2:p.Leu15= | |
| NM_001284290.2:c.45G>A | NP_001271219.1:p.Leu15= | |
| NM_001293104.2:c.-341G>A | NP_001280033.1:n.-341G>A | |
| NM_001293105.2:c.-285G>A | NP_001280034.1:n.-285G>A | |
| NR_120531.2:n.75G>A |