HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44352029G= , CM000679.2:g.44352029G= | GRCh38 |
NC_000017.10:g.42429397G= , CM000679.1:g.42429397G= | GRCh37 |
NC_000017.9:g.39784923G= | NCBI36 |
NG_007886.1:g.11907G= , LRG_661:g.11907G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000053867.8:c.1194G= MANE Select | ENSP00000053867.2:p.Ser398= | |
ENST00000639447.1:c.1136+277G= | ENSP00000492014.1:n.1136+277G= | |
ENST00000053867.7:c.1194G= | ENSP00000053867.2:p.Ser398= | |
ENST00000586443.1:c.635G= | ||
ENST00000589265.5:c.723G= | ENSP00000467616.1:p.Ser241= | |
NM_002087.3:c.1194G= | NP_002078.1:p.Ser398= | |
XM_005257253.1:c.1194G= | XP_005257310.1:p.Ser398= | |
XM_024450730.1:c.1194G= | XP_024306498.1:p.Ser398= | |
NM_002087.4:c.1194G= MANE Select | NP_002078.1:p.Ser398= |