Linked Data
ClinVar Variation Id:
15860
ClinVar RCV Id:
RCV000017206
dbSNP Id:
rs28928880
gnomAD v4:
16-176790-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.176790A>G , CM000678.2:g.176790A>G | GRCh38 |
| NC_000016.9:g.226789A>G , CM000678.1:g.226789A>G | GRCh37 |
| NC_000016.8:g.166789A>G | NCBI36 |
| NG_000006.1:g.37653A>G | |
| NG_059186.1:g.5140A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320868.9:c.74A>G MANE Select | ENSP00000322421.5:p.Tyr25Cys | |
| ENST00000397797.1:c.-2+28A>G | ENSP00000380899.1:n.-2+28A>G | |
| ENST00000472694.1:n.93A>G | ||
| ENST00000487791.1:n.43A>G | ||
| NM_000558.4:c.74A>G | NP_000549.1:p.Tyr25Cys | |
| NM_000558.5:c.74A>G MANE Select | NP_000549.1:p.Tyr25Cys |