HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56124537G>A , CM000674.2:g.56124537G>A | GRCh38 |
NC_000012.11:g.56518321G>A , CM000674.1:g.56518321G>A | GRCh37 |
NC_000012.10:g.54804588G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000257940.7:c.*2670G>A (ZC3H10) MANE Select | ENSP00000257940.2:n.*2670G>A | |
ENST00000257940.6:c.*2670G>A (ZC3H10) | ENSP00000257940.2:n.*2670G>A | |
ENST00000551790.5:c.-143-4003G>A (ESYT1) | ENSP00000447756.1:n.-143-4003G>A | |
NM_032786.3:c.*2670G>A (ZC3H10) MANE Select | NP_116175.1:n.*2670G>A | |
NM_001303124.2:c.*2670G>A (ZC3H10) | NP_001290053.1:n.*2670G>A | |
NM_001303125.2:c.*2670G>A (ZC3H10) | NP_001290054.1:n.*2670G>A |