Linked Data
ClinVar Variation Id:
2058988
ClinVar RCV Id:
RCV002952567
dbSNP Id:
rs756267462
gnomAD v2:
19-18266981-G-A
gnomAD v3:
19-18156171-G-A
gnomAD v4:
19-18156171-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18156171G>A , CM000681.2:g.18156171G>A | GRCh38 |
| NC_000019.9:g.18266981G>A , CM000681.1:g.18266981G>A | GRCh37 |
| NC_000019.8:g.18127981G>A | NCBI36 |
| NG_033010.1:g.7994G>A | |
| NG_033010.2:g.7994G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222254.13:c.292G>A MANE Select | ENSP00000222254.6:p.Ala98Thr | |
| ENST00000617130.5:c.292G>A | ENSP00000477864.2:p.Ala98Thr | |
| ENST00000617642.2:c.292G>A | ENSP00000484714.2:p.Ala98Thr | |
| ENST00000222254.12:c.292G>A | ENSP00000222254.6:p.Ala98Thr | |
| ENST00000426902.5:c.292G>A | ENSP00000395636.1:p.Ala98Thr | |
| ENST00000593731.1:c.292G>A | ENSP00000471914.1:p.Ala98Thr | |
| ENST00000617130.4:c.292G>A | ENSP00000477864.1:p.Ala98Thr | |
| ENST00000617642.1:c.292G>A | ENSP00000484714.1:p.Ala98Thr | |
| NM_005027.3:c.292G>A | NP_005018.1:p.Ala98Thr | |
| NR_073517.1:n.832G>A | ||
| NM_005027.4:c.292G>A MANE Select | NP_005018.2:p.Ala98Thr | |
| NR_073517.2:n.847G>A | ||
| NR_162071.1:n.847G>A |