HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196995754C= , CM000663.2:g.196995754C= | GRCh38 |
NC_000001.10:g.196964884C= , CM000663.1:g.196964884C= | GRCh37 |
NC_000001.9:g.195231507C= | NCBI36 |
NG_016365.1:g.23218C= , LRG_227:g.23218C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.390C= | ENSP00000514393.1:p.Ser130= | |
ENST00000699467.1:n.714C= | ||
ENST00000699468.1:c.-24-360C= | ENSP00000514394.1:n.-24-360C= | |
ENST00000256785.5:c.645C= MANE Select | ENSP00000256785.4:p.Ser215= | |
ENST00000256785.4:c.645C= | ENSP00000256785.4:p.Ser215= | |
NM_030787.3:c.645C= , LRG_227t1:c.645C= | NP_110414.1:p.Ser215= | |
XM_011510020.1:c.654C= | XP_011508322.1:p.Ser218= | |
XM_011510020.2:c.654C= | XP_011508322.1:p.Ser218= | |
NM_030787.4:c.645C= MANE Select | NP_110414.1:p.Ser215= |