Linked Data
ClinVar Variation Id:
3032428
ClinVar RCV Id:
RCV004534603
dbSNP Id:
rs867126915
gnomAD v4:
15-67066211-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.67066211G>A , CM000677.2:g.67066211G>A | GRCh38 |
| NC_000015.9:g.67358549G>A , CM000677.1:g.67358549G>A | GRCh37 |
| NC_000015.8:g.65145603G>A | NCBI36 |
| NG_011990.1:g.5355G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559460.6:c.-110+2267G>A | ENSP00000453082.2:n.-110+2267G>A | |
| ENST00000560424.2:c.57G>A | ENSP00000455540.2:p.Lys19= | |
| ENST00000327367.9:c.57G>A MANE Select | ENSP00000332973.4:p.Lys19= | |
| ENST00000327367.8:c.57G>A | ENSP00000332973.4:p.Lys19= | |
| ENST00000559460.5:c.-110+2267G>A | ENSP00000453082.1:n.-110+2267G>A | |
| NM_005902.3:c.57G>A | NP_005893.1:p.Lys19= | |
| XM_011521559.1:c.57G>A | XP_011519861.1:p.Lys19= | |
| XM_011521559.3:c.57G>A | XP_011519861.1:p.Lys19= | |
| NM_005902.4:c.57G>A MANE Select | NP_005893.1:p.Lys19= |