HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131877149A>C , CM000668.2:g.131877149A>C | GRCh38 |
NC_000006.11:g.132198289A>C , CM000668.1:g.132198289A>C | GRCh37 |
NC_000006.10:g.132239982A>C | NCBI36 |
NG_008206.1:g.74134A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000683687.1:n.753A>C | ||
ENST00000684536.1:n.379A>C | ||
ENST00000647893.1:c.1881A>C MANE Select | ENSP00000498074.1:p.Ser627= | |
ENST00000647981.1:n.566A>C | ||
ENST00000650437.1:c.1372A>C | ||
ENST00000360971.6:c.1881A>C | ENSP00000354238.2:p.Ser627= | |
ENST00000459624.1:n.925A>C | ||
ENST00000513998.5:c.*718A>C | ENSP00000422424.1:n.*718A>C | |
NM_006208.2:c.1881A>C | NP_006199.2:p.Ser627= | |
XM_011535896.1:c.771A>C | XP_011534198.1:p.Ser257= | |
NM_006208.3:c.1881A>C MANE Select | NP_006199.2:p.Ser627= |