HGVS | Genome Assembly |
---|---|
NC_000001.11:g.147908297G= , CM000663.2:g.147908297G= | GRCh38 |
NC_000001.10:g.147380424G= , CM000663.1:g.147380424G= | GRCh37 |
NC_000001.9:g.145847048G= | NCBI36 |
NG_016242.1:g.10479G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369235.2:c.342G= MANE Select | ENSP00000358238.1:p.Leu114= | |
ENST00000369235.1:c.342G= | ENSP00000358238.1:p.Leu114= | |
NM_005267.4:c.342G= | NP_005258.2:p.Leu114= | |
XM_011509416.1:c.342G= | XP_011507718.1:p.Leu114= | |
XM_011509417.1:c.342G= | XP_011507719.1:p.Leu114= | |
XM_011509417.2:c.342G= | XP_011507719.1:p.Leu114= | |
XR_002956281.1:n.1257G= | ||
NM_005267.5:c.342G= MANE Select | NP_005258.2:p.Leu114= |