HGVS | Genome Assembly |
---|---|
NC_000014.9:g.91272716C= , CM000676.2:g.91272716C= | GRCh38 |
NC_000014.8:g.91739060C= , CM000676.1:g.91739060C= | GRCh37 |
NC_000014.7:g.90808813C= | NCBI36 |
NG_033118.1:g.150129G= | |
NG_033118.2:g.150129G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389857.11:c.5996G= MANE Select | ENSP00000374507.6:p.Cys1999= | |
ENST00000331194.8:c.1430G= | ENSP00000330332.8:p.Cys477= | |
ENST00000389857.10:c.5996G= | ENSP00000374507.6:p.Cys1999= | |
ENST00000556726.5:c.2224G= | ||
NM_001080414.3:c.5996G= | NP_001073883.2:p.Cys1999= | |
XM_011536796.1:c.5888G= | XP_011535098.1:p.Cys1963= | |
XM_011536796.2:c.5888G= | XP_011535098.1:p.Cys1963= | |
XM_017021336.1:c.3077G= | XP_016876825.1:p.Cys1026= | |
NM_001080414.4:c.5996G= MANE Select | NP_001073883.2:p.Cys1999= |