HGVS | Genome Assembly |
---|---|
NC_000007.14:g.37906782A>G , CM000669.2:g.37906782A>G | GRCh38 |
NC_000007.13:g.37946384A>G , CM000669.1:g.37946384A>G | GRCh37 |
NC_000007.12:g.37912909A>G | NCBI36 |
NG_052980.1:g.15142T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000436072.7:c.*697T>C (SFRP4) MANE Select | ENSP00000410715.2:n.*697T>C | |
ENST00000436072.6:c.*697T>C (SFRP4) | ENSP00000410715.2:n.*697T>C | |
ENST00000476620.1:c.-37-42058A>G (EPDR1) | ENSP00000425858.1:n.-37-42058A>G | |
NM_003014.3:c.*697T>C (SFRP4) | NP_003005.2:n.*697T>C | |
NM_003014.4:c.*697T>C (SFRP4) MANE Select | NP_003005.2:n.*697T>C |