HGVS | Genome Assembly |
---|---|
NC_000001.11:g.40838388C>T , CM000663.2:g.40838388C>T | GRCh38 |
NC_000001.10:g.41304060C>T , CM000663.1:g.41304060C>T | GRCh37 |
NC_000001.9:g.41076647C>T | NCBI36 |
NG_008139.1:g.59377C>T | |
NG_008139.2:g.59377C>T | |
NG_008139.3:g.59602C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000347132.10:c.1953C>T MANE Select | ENSP00000262916.6:p.Ser651= | |
ENST00000347132.9:c.1953C>T | ENSP00000262916.6:p.Ser651= | |
ENST00000443478.3:c.1534C>T | ||
ENST00000506017.1:n.1272C>T | ||
ENST00000509682.6:c.1791C>T | ENSP00000423756.2:p.Ser597= | |
NM_004700.3:c.1953C>T | NP_004691.2:p.Ser651= | |
NM_172163.2:c.1791C>T | NP_751895.1:p.Ser597= | |
XM_017002792.1:c.936C>T | XP_016858281.1:p.Ser312= | |
NM_004700.4:c.1953C>T MANE Select | NP_004691.2:p.Ser651= | |
NM_172163.3:c.1791C>T | NP_751895.1:p.Ser597= |