HGVS | Genome Assembly |
---|---|
NC_000010.11:g.72007968G>T , CM000672.2:g.72007968G>T | GRCh38 |
NC_000010.10:g.73767726G>T , CM000672.1:g.73767726G>T | GRCh37 |
NC_000010.9:g.73437732G>T | NCBI36 |
NG_012635.1:g.48607G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373115.5:c.937G>T MANE Select | ENSP00000362207.4:p.Ala313Ser | |
ENST00000373115.4:c.937G>T | ENSP00000362207.4:p.Ala313Ser | |
NM_004273.4:c.937G>T | NP_004264.2:p.Ala313Ser | |
XM_006718075.2:c.937G>T | XP_006718138.1:p.Ala313Ser | |
XM_011540369.1:c.937G>T | XP_011538671.1:p.Ala313Ser | |
XM_006718075.4:c.937G>T | XP_006718138.1:p.Ala313Ser | |
XM_011540369.2:c.937G>T | XP_011538671.1:p.Ala313Ser | |
NM_004273.5:c.937G>T MANE Select | NP_004264.2:p.Ala313Ser |