HGVS | Genome Assembly |
---|---|
NC_000014.9:g.91272911G>T , CM000676.2:g.91272911G>T | GRCh38 |
NC_000014.8:g.91739255G>T , CM000676.1:g.91739255G>T | GRCh37 |
NC_000014.7:g.90809008G>T | NCBI36 |
NG_033118.1:g.149934C>A | |
NG_033118.2:g.149934C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389857.11:c.5801C>A MANE Select | ENSP00000374507.6:p.Ala1934Asp | |
ENST00000331194.8:c.1235C>A | ENSP00000330332.8:p.Ala412Asp | |
ENST00000389857.10:c.5801C>A | ENSP00000374507.6:p.Ala1934Asp | |
ENST00000556726.5:c.2029C>A | ||
NM_001080414.3:c.5801C>A | NP_001073883.2:p.Ala1934Asp | |
XM_011536796.1:c.5693C>A | XP_011535098.1:p.Ala1898Asp | |
XM_011536796.2:c.5693C>A | XP_011535098.1:p.Ala1898Asp | |
XM_017021336.1:c.2882C>A | XP_016876825.1:p.Ala961Asp | |
NM_001080414.4:c.5801C>A MANE Select | NP_001073883.2:p.Ala1934Asp |