Linked Data
ClinVar Variation Id:
899608
dbSNP Id:
rs72646292
ExAC:
4:187130365 T / C
gnomAD v2:
4-187130365-T-C
gnomAD v3:
4-186209211-T-C
gnomAD v4:
4-186209211-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186209211T>C , CM000666.2:g.186209211T>C | GRCh38 |
| NC_000004.11:g.187130365T>C , CM000666.1:g.187130365T>C | GRCh37 |
| NC_000004.10:g.187367359T>C | NCBI36 |
| NG_007965.1:g.22692T>C | |
| NG_012095.2:g.5233T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378802.5:c.1344T>C (CYP4V2) MANE Select | ENSP00000368079.4:p.Asn448= | |
| ENST00000378802.4:c.1344T>C (CYP4V2) | ENSP00000368079.4:p.Asn448= | |
| ENST00000502665.1:n.579T>C (CYP4V2) | ||
| ENST00000507209.5:n.6042T>C (CYP4V2) | ||
| ENST00000511608.5:c.140T>C (KLKB1) | ||
| ENST00000513354.5:n.434T>C (CYP4V2) | ||
| NM_207352.3:c.1344T>C (CYP4V2) | NP_997235.3:p.Asn448= | |
| XM_005262935.2:c.1341T>C (CYP4V2) | XP_005262992.1:p.Asn447= | |
| XM_006714184.2:c.948T>C (CYP4V2) | XP_006714247.1:p.Asn316= | |
| XM_005262935.4:c.1341T>C (CYP4V2) | XP_005262992.1:p.Asn447= | |
| XM_017008037.1:c.948T>C (CYP4V2) | XP_016863526.1:p.Asn316= | |
| NM_207352.4:c.1344T>C (CYP4V2) MANE Select | NP_997235.3:p.Asn448= |