HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154996977A= , CM000685.2:g.154996977A= | GRCh38 |
NC_000023.10:g.154225252A= , CM000685.1:g.154225252A= | GRCh37 |
NC_000023.9:g.153878446A= | NCBI36 |
NG_011403.1:g.30747T= | |
NG_011403.2:g.30747T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.384T= MANE Select | ENSP00000353393.4:p.Ser128= | |
ENST00000647125.1:c.*170T= | ENSP00000496062.1:n.*170T= | |
ENST00000360256.8:c.384T= | ENSP00000353393.4:p.Ser128= | |
ENST00000423959.5:c.279T= | ENSP00000409446.1:p.Ser93= | |
ENST00000453950.1:c.366T= | ENSP00000389153.1:p.Ser122= | |
NM_000132.3:c.384T= | NP_000123.1:p.Ser128= | |
XM_011531126.1:c.279T= | XP_011529428.1:p.Ser93= | |
NM_000132.4:c.384T= MANE Select | NP_000123.1:p.Ser128= |