Linked Data
ClinVar Variation Id:
429639
dbSNP Id:
rs1131691504
gnomAD v2:
19-39055815-G-A
gnomAD v4:
19-38565175-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38565175G>A , CM000681.2:g.38565175G>A | GRCh38 |
| NC_000019.9:g.39055815G>A , CM000681.1:g.39055815G>A | GRCh37 |
| NC_000019.8:g.43747655G>A | NCBI36 |
| NG_008866.1:g.136476G>A , LRG_766:g.136476G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000688602.1:c.1251G>A | ||
| ENST00000689936.1:c.1233G>A | ||
| ENST00000359596.8:c.12841G>A MANE Select | ENSP00000352608.2:p.Gly4281Arg | |
| ENST00000355481.8:c.12826G>A | ENSP00000347667.3:p.Gly4276Arg | |
| ENST00000359596.7:c.12841G>A | ENSP00000352608.2:p.Gly4281Arg | |
| ENST00000360985.7:c.12823G>A | ENSP00000354254.4:p.Gly4275Arg | |
| ENST00000594335.5:c.6210G>A | ||
| NM_000540.2:c.12841G>A , LRG_766t1:c.12841G>A | NP_000531.2:p.Gly4281Arg | |
| NM_001042723.1:c.12826G>A | NP_001036188.1:p.Gly4276Arg | |
| XM_006723317.1:c.12823G>A | XP_006723380.1:p.Gly4275Arg | |
| XM_006723319.1:c.12808G>A | XP_006723382.1:p.Gly4270Arg | |
| XM_011527204.1:c.12838G>A | XP_011525506.1:p.Gly4280Arg | |
| XM_011527205.1:c.12841G>A | XP_011525507.1:p.Gly4281Arg | |
| XM_006723317.2:c.12823G>A | XP_006723380.1:p.Gly4275Arg | |
| XM_006723319.2:c.12808G>A | XP_006723382.1:p.Gly4270Arg | |
| XM_011527205.2:c.12841G>A | XP_011525507.1:p.Gly4281Arg | |
| NM_000540.3:c.12841G>A MANE Select | NP_000531.2:p.Gly4281Arg | |
| NM_001042723.2:c.12826G>A | NP_001036188.1:p.Gly4276Arg |