HGVS | Genome Assembly |
---|---|
NC_000016.10:g.84907723C>T , CM000678.2:g.84907723C>T | GRCh38 |
NC_000016.9:g.84941329C>T , CM000678.1:g.84941329C>T | GRCh37 |
NC_000016.8:g.83498830C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262424.10:c.*1081C>T MANE Select | ENSP00000262424.5:n.*1081C>T | |
ENST00000262424.9:c.*1081C>T | ENSP00000262424.5:n.*1081C>T | |
ENST00000566165.1:c.121-11917C>T | ||
NM_031476.3:c.*1081C>T | NP_113664.1:n.*1081C>T | |
XM_005256190.1:c.*1081C>T | XP_005256247.1:n.*1081C>T | |
NM_031476.4:c.*1081C>T MANE Select | NP_113664.1:n.*1081C>T |