HGVS | Genome Assembly |
---|---|
NC_000008.11:g.37966075G= , CM000670.2:g.37966075G= | GRCh38 |
NC_000008.10:g.37823593G= , CM000670.1:g.37823593G= | GRCh37 |
NC_000008.9:g.37942750G= | NCBI36 |
NG_011936.1:g.5592C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000345060.5:c.395C= MANE Select | ENSP00000343782.3:p.Ala132= | |
ENST00000520341.2:n.523C= | ||
ENST00000345060.4:c.395C= | ENSP00000343782.3:p.Ala132= | |
ENST00000614635.1:c.395C= | ENSP00000480325.1:p.Ala132= | |
NM_000025.2:c.395C= | NP_000016.1:p.Ala132= | |
NM_000025.3:c.395C= MANE Select | NP_000016.1:p.Ala132= |