Linked Data
ClinVar Variation Id:
892851
dbSNP Id:
rs959737076
gnomAD v2:
19-39075709-G-A
gnomAD v4:
19-38585069-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38585069G>A , CM000681.2:g.38585069G>A | GRCh38 |
| NC_000019.9:g.39075709G>A , CM000681.1:g.39075709G>A | GRCh37 |
| NC_000019.8:g.43767549G>A | NCBI36 |
| NG_008866.1:g.156370G>A , LRG_766:g.156370G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.1709G>A | ||
| ENST00000688602.1:c.3106G>A | ||
| ENST00000689936.1:c.3078G>A | ||
| ENST00000692547.1:n.166G>A | ||
| ENST00000359596.8:c.14773G>A MANE Select | ENSP00000352608.2:p.Val4925Ile | |
| ENST00000355481.8:c.14758G>A | ENSP00000347667.3:p.Val4920Ile | |
| ENST00000359596.7:c.14773G>A | ENSP00000352608.2:p.Val4925Ile | |
| ENST00000360985.7:c.14755G>A | ENSP00000354254.4:p.Val4919Ile | |
| NM_000540.2:c.14773G>A , LRG_766t1:c.14773G>A | NP_000531.2:p.Val4925Ile | |
| NM_001042723.1:c.14758G>A | NP_001036188.1:p.Val4920Ile | |
| XM_006723317.1:c.14755G>A | XP_006723380.1:p.Val4919Ile | |
| XM_006723319.1:c.14740G>A | XP_006723382.1:p.Val4914Ile | |
| XM_011527204.1:c.14770G>A | XP_011525506.1:p.Val4924Ile | |
| XM_011527205.1:c.14686G>A | XP_011525507.1:p.Val4896Ile | |
| XM_006723317.2:c.14755G>A | XP_006723380.1:p.Val4919Ile | |
| XM_006723319.2:c.14740G>A | XP_006723382.1:p.Val4914Ile | |
| XM_011527205.2:c.14686G>A | XP_011525507.1:p.Val4896Ile | |
| NM_000540.3:c.14773G>A MANE Select | NP_000531.2:p.Val4925Ile | |
| NM_001042723.2:c.14758G>A | NP_001036188.1:p.Val4920Ile |