HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2340593G= , CM000678.2:g.2340593G= | GRCh38 |
NC_000016.9:g.2390594G= , CM000678.1:g.2390594G= | GRCh37 |
NC_000016.8:g.2330595G= | NCBI36 |
NG_011790.1:g.5154C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301732.10:c.-559C= (ABCA3) MANE Select | ENSP00000301732.5:n.-559C= | |
ENST00000640929.1:n.42+1262G= (ABCA17P) | ||
ENST00000301732.9:c.-559C= (ABCA3) | ENSP00000301732.5:n.-559C= | |
ENST00000382381.7:c.-559C= (ABCA3) | ENSP00000371818.3:n.-559C= | |
ENST00000512848.5:n.182+1262G= (ABCA17P) | ||
ENST00000563623.5:n.5C= (ABCA3) | ||
NM_001089.2:c.-559C= (ABCA3) | NP_001080.2:n.-559C= | |
NM_001089.3:c.-559C= (ABCA3) MANE Select | NP_001080.2:n.-559C= |