HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87727523A>G , CM000672.2:g.87727523A>G | GRCh38 |
NC_000010.10:g.89487280A>G , CM000672.1:g.89487280A>G | GRCh37 |
NC_000010.9:g.89477260A>G | NCBI36 |
NG_012150.1:g.72805A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000456849.2:c.1086+34A>G MANE Select | ENSP00000406157.1:n.1086+34A>G | |
ENST00000361175.8:c.1071+34A>G | ENSP00000354436.4:n.1071+34A>G | |
ENST00000456849.1:c.1086+34A>G | ENSP00000406157.1:n.1086+34A>G | |
NM_001015880.1:c.1086+34A>G | NP_001015880.1:n.1086+34A>G | |
NM_004670.3:c.1071+34A>G | NP_004661.2:n.1071+34A>G | |
NM_001015880.2:c.1086+34A>G MANE Select | NP_001015880.1:n.1086+34A>G | |
NM_004670.4:c.1071+34A>G | NP_004661.2:n.1071+34A>G |