HGVS | Genome Assembly |
---|---|
NC_000007.14:g.37906760T>A , CM000669.2:g.37906760T>A | GRCh38 |
NC_000007.13:g.37946362T>A , CM000669.1:g.37946362T>A | GRCh37 |
NC_000007.12:g.37912887T>A | NCBI36 |
NG_052980.1:g.15164A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000436072.7:c.*719A>T (SFRP4) MANE Select | ENSP00000410715.2:n.*719A>T | |
ENST00000436072.6:c.*719A>T (SFRP4) | ENSP00000410715.2:n.*719A>T | |
ENST00000476620.1:c.-37-42080T>A (EPDR1) | ENSP00000425858.1:n.-37-42080T>A | |
NM_003014.3:c.*719A>T (SFRP4) | NP_003005.2:n.*719A>T | |
NM_003014.4:c.*719A>T (SFRP4) MANE Select | NP_003005.2:n.*719A>T |