HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131851278C>T , CM000668.2:g.131851278C>T | GRCh38 |
NC_000006.11:g.132172418C>T , CM000668.1:g.132172418C>T | GRCh37 |
NC_000006.10:g.132214111C>T | NCBI36 |
NG_008206.1:g.48263C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647893.1:c.556+11C>T MANE Select | ENSP00000498074.1:n.556+11C>T | |
ENST00000650147.1:c.234+11C>T | ||
ENST00000650437.1:c.108+1172C>T | ||
ENST00000360971.6:c.556+11C>T | ENSP00000354238.2:n.556+11C>T | |
ENST00000486853.1:n.587C>T | ||
ENST00000513998.5:c.556+11C>T | ENSP00000422424.1:n.556+11C>T | |
NM_006208.2:c.556+11C>T | NP_006199.2:n.556+11C>T | |
NM_006208.3:c.556+11C>T MANE Select | NP_006199.2:n.556+11C>T |