Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.37907501C= , CM000669.2:g.37907501C= | GRCh38 |
| NC_000007.13:g.37947103C= , CM000669.1:g.37947103C= | GRCh37 |
| NC_000007.12:g.37913628C= | NCBI36 |
| NG_052980.1:g.14423G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003014.4:c.1019G= (SFRP4) MANE Select | NP_003005.2:p.Arg340= |
| ENST00000436072.7:c.1019G= (SFRP4) MANE Select | ENSP00000410715.2:p.Arg340= |
| NM_003014.3:c.1019G= (SFRP4) | NP_003005.2:p.Arg340= |
| ENST00000436072.6:c.1019G= (SFRP4) | ENSP00000410715.2:p.Arg340= |
| ENST00000476620.1:c.-37-41339C= (EPDR1) | ENSP00000425858.1:n.-37-41339C= |
| ENST00000478975.1:n.387G= (SFRP4) |