HGVS | Genome Assembly |
---|---|
NC_000014.9:g.91272632C>T , CM000676.2:g.91272632C>T | GRCh38 |
NC_000014.8:g.91738976C>T , CM000676.1:g.91738976C>T | GRCh37 |
NC_000014.7:g.90808729C>T | NCBI36 |
NG_033118.1:g.150213G>A | |
NG_033118.2:g.150213G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389857.11:c.6080G>A MANE Select | ENSP00000374507.6:p.Cys2027Tyr | |
ENST00000331194.8:c.1514G>A | ENSP00000330332.8:p.Cys505Tyr | |
ENST00000389857.10:c.6080G>A | ENSP00000374507.6:p.Cys2027Tyr | |
ENST00000556726.5:c.2308G>A | ||
NM_001080414.3:c.6080G>A | NP_001073883.2:p.Cys2027Tyr | |
XM_011536796.1:c.5972G>A | XP_011535098.1:p.Cys1991Tyr | |
XM_011536796.2:c.5972G>A | XP_011535098.1:p.Cys1991Tyr | |
XM_017021336.1:c.3161G>A | XP_016876825.1:p.Cys1054Tyr | |
NM_001080414.4:c.6080G>A MANE Select | NP_001073883.2:p.Cys2027Tyr |