HGVS | Genome Assembly |
---|---|
NC_000010.11:g.72007538G>C , CM000672.2:g.72007538G>C | GRCh38 |
NC_000010.10:g.73767296G>C , CM000672.1:g.73767296G>C | GRCh37 |
NC_000010.9:g.73437302G>C | NCBI36 |
NG_012635.1:g.48177G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373115.5:c.507G>C MANE Select | ENSP00000362207.4:p.Glu169Asp | |
ENST00000373115.4:c.507G>C | ENSP00000362207.4:p.Glu169Asp | |
NM_004273.4:c.507G>C | NP_004264.2:p.Glu169Asp | |
XM_006718075.2:c.507G>C | XP_006718138.1:p.Glu169Asp | |
XM_011540369.1:c.507G>C | XP_011538671.1:p.Glu169Asp | |
XM_006718075.4:c.507G>C | XP_006718138.1:p.Glu169Asp | |
XM_011540369.2:c.507G>C | XP_011538671.1:p.Glu169Asp | |
NM_004273.5:c.507G>C MANE Select | NP_004264.2:p.Glu169Asp |