HGVS | Genome Assembly |
---|---|
NC_000005.10:g.132656929G>A , CM000667.2:g.132656929G>A | GRCh38 |
NC_000005.9:g.131992621G>A , CM000667.1:g.131992621G>A | GRCh37 |
NC_000005.8:g.132020520G>A | NCBI36 |
NG_012090.1:g.3757G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000459878.5:n.107+299G>A | ||
ENST00000468334.5:n.369-137G>A | ||
ENST00000487267.5:n.96-137G>A | ||
NM_001354991.1:c.-93+299G>A | NP_001341920.1:n.-93+299G>A | |
NM_001354992.1:c.-271-137G>A | NP_001341921.1:n.-271-137G>A | |
NM_001354993.1:c.-200-137G>A | NP_001341922.1:n.-200-137G>A | |
NM_001354991.2:c.-93+299G>A | NP_001341920.1:n.-93+299G>A | |
NM_001354992.2:c.-271-137G>A | NP_001341921.1:n.-271-137G>A | |
NM_001354993.2:c.-200-137G>A | NP_001341922.1:n.-200-137G>A |