Linked Data
gnomAD v4:
7-37906897-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.37906897T>A , CM000669.2:g.37906897T>A | GRCh38 |
| NC_000007.13:g.37946499T>A , CM000669.1:g.37946499T>A | GRCh37 |
| NC_000007.12:g.37913024T>A | NCBI36 |
| NG_052980.1:g.15027A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436072.7:c.*582A>T (SFRP4) MANE Select | ENSP00000410715.2:n.*582A>T | |
| ENST00000436072.6:c.*582A>T (SFRP4) | ENSP00000410715.2:n.*582A>T | |
| ENST00000476620.1:c.-37-41943T>A (EPDR1) | ENSP00000425858.1:n.-37-41943T>A | |
| NM_003014.3:c.*582A>T (SFRP4) | NP_003005.2:n.*582A>T | |
| NM_003014.4:c.*582A>T (SFRP4) MANE Select | NP_003005.2:n.*582A>T |