HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56124624T>G , CM000674.2:g.56124624T>G | GRCh38 |
NC_000012.11:g.56518408T>G , CM000674.1:g.56518408T>G | GRCh37 |
NC_000012.10:g.54804675T>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000257940.7:c.*2757T>G (ZC3H10) MANE Select | ENSP00000257940.2:n.*2757T>G | |
ENST00000257940.6:c.*2757T>G (ZC3H10) | ENSP00000257940.2:n.*2757T>G | |
ENST00000551790.5:c.-143-3916T>G (ESYT1) | ENSP00000447756.1:n.-143-3916T>G | |
NM_032786.3:c.*2757T>G (ZC3H10) MANE Select | NP_116175.1:n.*2757T>G | |
NM_001303124.2:c.*2757T>G (ZC3H10) | NP_001290053.1:n.*2757T>G | |
NM_001303125.2:c.*2757T>G (ZC3H10) | NP_001290054.1:n.*2757T>G |