Linked Data
dbSNP Id:
rs10484410
gnomAD v2:
6-56996688-T-C
gnomAD v3:
6-57131890-T-C
gnomAD v4:
6-57131890-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.57131890T>C , CM000668.2:g.57131890T>C | GRCh38 |
| NC_000006.11:g.56996688T>C , CM000668.1:g.56996688T>C | GRCh37 |
| NC_000006.10:g.57104647T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370706.9:c.425-1152T>C (ZNF451) MANE Select | ENSP00000359740.4:n.425-1152T>C | |
| ENST00000357489.7:c.425-1152T>C (ZNF451) | ENSP00000350083.3:n.425-1152T>C | |
| ENST00000370706.8:c.425-1152T>C (ZNF451) | ENSP00000359740.4:n.425-1152T>C | |
| ENST00000444273.6:n.566-1152T>C (ZNF451) | ||
| ENST00000491832.6:c.425-1152T>C (ZNF451) | ENSP00000421645.1:n.425-1152T>C | |
| ENST00000502749.1:c.*184-1152T>C (ZNF451) | ENSP00000424329.1:n.*184-1152T>C | |
| ENST00000504603.1:c.106-10058T>C (ZNF451) | ENSP00000425047.1:n.106-10058T>C | |
| ENST00000510483.5:c.341-1152T>C (ZNF451) | ENSP00000427558.1:n.341-1152T>C | |
| ENST00000515290.5:c.8-1152T>C (ZNF451) | ENSP00000424723.1:n.8-1152T>C | |
| NM_001031623.2:c.425-1152T>C (ZNF451) | NP_001026794.1:n.425-1152T>C | |
| NM_015555.2:c.425-1152T>C (ZNF451) | NP_056370.2:n.425-1152T>C | |
| NR_110742.1:n.235-16327A>G (ZNF451-AS1) | ||
| XM_005248994.1:c.425-1152T>C (ZNF451) | XP_005249051.1:n.425-1152T>C | |
| XM_011514460.1:c.341-1152T>C (ZNF451) | XP_011512762.1:n.341-1152T>C | |
| XM_011514461.1:c.275-1152T>C (ZNF451) | XP_011512763.1:n.275-1152T>C | |
| XM_011514462.1:c.425-1152T>C (ZNF451) | XP_011512764.1:n.425-1152T>C | |
| XR_241885.1:n.669-1152T>C (ZNF451) | ||
| XM_005248994.2:c.425-1152T>C (ZNF451) | XP_005249051.1:n.425-1152T>C | |
| XM_011514460.2:c.341-1152T>C (ZNF451) | XP_011512762.1:n.341-1152T>C | |
| XM_011514461.2:c.275-1152T>C (ZNF451) | XP_011512763.1:n.275-1152T>C | |
| XM_011514462.3:c.425-1152T>C (ZNF451) | XP_011512764.1:n.425-1152T>C | |
| XR_001743327.2:n.3986-1152T>C (ZNF451) | ||
| XR_001743329.1:n.2703-1152T>C (ZNF451) | ||
| XR_241885.2:n.639-1152T>C (ZNF451) | ||
| NM_001031623.3:c.425-1152T>C (ZNF451) MANE Select | NP_001026794.1:n.425-1152T>C | |
| NM_015555.3:c.425-1152T>C (ZNF451) | NP_056370.2:n.425-1152T>C |