HGVS | Genome Assembly |
---|---|
NC_000016.10:g.22877877A>C , CM000678.2:g.22877877A>C | GRCh38 |
NC_000016.9:g.22889198A>C , CM000678.1:g.22889198A>C | GRCh37 |
NC_000016.8:g.22796699A>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261374.4:c.486-37067A>C MANE Select | ENSP00000261374.3:n.486-37067A>C | |
ENST00000261374.3:c.486-37067A>C | ENSP00000261374.3:n.486-37067A>C | |
ENST00000473392.1:c.*287+23096A>C | ENSP00000454505.1:n.*287+23096A>C | |
NM_006043.1:c.486-37067A>C | NP_006034.1:n.486-37067A>C | |
NM_006043.2:c.486-37067A>C MANE Select | NP_006034.1:n.486-37067A>C |