Linked Data
ClinVar Variation Id:
2280308
ClinVar RCV Id:
RCV004135646
dbSNP Id:
rs949891831
gnomAD v2:
1-247201082-G-A
gnomAD v3:
1-247037780-G-A
gnomAD v4:
1-247037780-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.247037780G>A , CM000663.2:g.247037780G>A | GRCh38 |
| NC_000001.10:g.247201082G>A , CM000663.1:g.247201082G>A | GRCh37 |
| NC_000001.9:g.245267705G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366503.3:c.839C>T (ZNF670) MANE Select | ENSP00000355459.2:p.Pro280Leu | |
| ENST00000366503.2:c.839C>T (ZNF670) | ENSP00000355459.2:p.Pro280Leu | |
| ENST00000465049.6:c.4-37706C>T (ZNF670-ZNF695) | ENSP00000428213.1:n.4-37706C>T | |
| ENST00000474541.1:c.4-37706C>T (ZNF670-ZNF695) | ENSP00000428036.1:n.4-37706C>T | |
| NM_001204220.1:c.836C>T (ZNF670) | NP_001191149.1:p.Pro279Leu | |
| NM_033213.4:c.839C>T (ZNF670) | NP_149990.1:p.Pro280Leu | |
| NR_037894.1:n.221-37706C>T (ZNF670-ZNF695) | ||
| NM_033213.5:c.839C>T (ZNF670) MANE Select | NP_149990.1:p.Pro280Leu | |
| NM_001204220.2:c.836C>T (ZNF670) | NP_001191149.1:p.Pro279Leu | |
| NR_037894.2:n.219-37706C>T (ZNF670-ZNF695) |