HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21880821C>T , CM000669.2:g.21880821C>T | GRCh38 |
NC_000007.13:g.21920439C>T , CM000669.1:g.21920439C>T | GRCh37 |
NC_000007.12:g.21886964C>T | NCBI36 |
NG_012886.2:g.342607C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.12315C>T MANE Select | ENSP00000475939.1:p.Ser4105= | |
ENST00000328843.10:c.12336C>T | ENSP00000330671.7:p.Ser4112= | |
ENST00000409508.7:c.12315C>T | ENSP00000475939.1:p.Ser4105= | |
ENST00000620169.4:c.12336C>T | ENSP00000481693.1:p.Ser4112= | |
NM_001277115.1:c.12315C>T | NP_001264044.1:p.Ser4105= | |
NM_001277115.2:c.12315C>T MANE Select | NP_001264044.1:p.Ser4105= |