HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2340629T>C , CM000678.2:g.2340629T>C | GRCh38 |
NC_000016.9:g.2390630T>C , CM000678.1:g.2390630T>C | GRCh37 |
NC_000016.8:g.2330631T>C | NCBI36 |
NG_011790.1:g.5118A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301732.10:c.-595A>G (ABCA3) MANE Select | ENSP00000301732.5:n.-595A>G | |
ENST00000640929.1:n.42+1298T>C (ABCA17P) | ||
ENST00000301732.9:c.-595A>G (ABCA3) | ENSP00000301732.5:n.-595A>G | |
ENST00000382381.7:c.-595A>G (ABCA3) | ENSP00000371818.3:n.-595A>G | |
ENST00000512848.5:n.182+1298T>C (ABCA17P) | ||
NM_001089.2:c.-595A>G (ABCA3) | NP_001080.2:n.-595A>G | |
NM_001089.3:c.-595A>G (ABCA3) MANE Select | NP_001080.2:n.-595A>G |