HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131877009C>T , CM000668.2:g.131877009C>T | GRCh38 |
NC_000006.11:g.132198149C>T , CM000668.1:g.132198149C>T | GRCh37 |
NC_000006.10:g.132239842C>T | NCBI36 |
NG_008206.1:g.73994C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000683687.1:n.613C>T | ||
ENST00000684536.1:n.239C>T | ||
ENST00000647893.1:c.1741C>T MANE Select | ENSP00000498074.1:p.Pro581Ser | |
ENST00000647981.1:n.426C>T | ||
ENST00000650437.1:c.1232C>T | ||
ENST00000360971.6:c.1741C>T | ENSP00000354238.2:p.Pro581Ser | |
ENST00000459624.1:n.785C>T | ||
ENST00000513998.5:c.*578C>T | ENSP00000422424.1:n.*578C>T | |
NM_006208.2:c.1741C>T | NP_006199.2:p.Pro581Ser | |
XM_011535896.1:c.631C>T | XP_011534198.1:p.Pro211Ser | |
NM_006208.3:c.1741C>T MANE Select | NP_006199.2:p.Pro581Ser |