Linked Data
ClinVar Variation Id:
1503656
ClinVar RCV Id:
RCV002045484
dbSNP Id:
rs2151070785
gnomAD v4:
6-35814563-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35814563G>A , CM000668.2:g.35814563G>A | GRCh38 |
| NC_000006.11:g.35782340G>A , CM000668.1:g.35782340G>A | GRCh37 |
| NC_000006.10:g.35890318G>A | NCBI36 |
| NG_012184.1:g.14270G>A | |
| NG_012184.2:g.14270G>A | |
| NG_012184.3:g.22358G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360215.3:c.430G>A MANE Select | ENSP00000353346.1:p.Gly144Ser | |
| ENST00000496656.2:n.209G>A | ||
| ENST00000651132.1:c.430G>A | ENSP00000498322.1:p.Gly144Ser | |
| ENST00000651676.1:c.430G>A | ENSP00000498699.1:p.Gly144Ser | |
| ENST00000651994.1:c.*70-4874G>A | ENSP00000498310.1:n.*70-4874G>A | |
| ENST00000652718.1:c.262G>A | ENSP00000498866.1:p.Gly88Ser | |
| ENST00000360215.2:c.430G>A | ENSP00000353346.1:p.Gly144Ser | |
| ENST00000496656.1:n.209G>A | ||
| NM_182548.3:c.430G>A | NP_872354.1:p.Gly144Ser | |
| XM_011514403.1:c.430G>A | XP_011512705.1:p.Gly144Ser | |
| NM_182548.4:c.430G>A MANE Select | NP_872354.1:p.Gly144Ser |