HGVS | Genome Assembly |
---|---|
NC_000023.11:g.108665560G>A , CM000685.2:g.108665560G>A | GRCh38 |
NC_000023.10:g.107908790G>A , CM000685.1:g.107908790G>A | GRCh37 |
NC_000023.9:g.107795446G>A | NCBI36 |
NG_011977.1:g.230637G>A | |
NG_011977.2:g.230637G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000328300.11:c.3427G>A MANE Select | ENSP00000331902.7:p.Gly1143Ser | |
ENST00000361603.7:c.3427G>A | ENSP00000354505.2:p.Gly1143Ser | |
ENST00000328300.10:c.3427G>A | ENSP00000331902.6:p.Gly1143Ser | |
ENST00000361603.6:c.3427G>A | ENSP00000354505.2:p.Gly1143Ser | |
NM_000495.4:c.3427G>A | NP_000486.1:p.Gly1143Ser | |
NM_033380.2:c.3427G>A | NP_203699.1:p.Gly1143Ser | |
XM_005262070.2:c.3427G>A | XP_005262127.1:p.Gly1143Ser | |
XM_006724616.2:c.3427G>A | XP_006724679.1:p.Gly1143Ser | |
XM_011530849.1:c.3103G>A | XP_011529151.1:p.Gly1035Ser | |
XM_011530850.1:c.3427G>A | XP_011529152.1:p.Gly1143Ser | |
XM_011530851.1:c.1000G>A | XP_011529153.1:p.Gly334Ser | |
XM_011530849.2:c.3442G>A | XP_011529151.2:p.Gly1148Ser | |
XM_017029259.2:c.3442G>A | XP_016884748.1:p.Gly1148Ser | |
XM_017029260.1:c.3442G>A | XP_016884749.1:p.Gly1148Ser | |
XM_017029261.1:c.3442G>A | XP_016884750.1:p.Gly1148Ser | |
XM_017029262.2:c.3442G>A | XP_016884751.1:p.Gly1148Ser | |
XM_017029263.2:c.1762G>A | XP_016884752.1:p.Gly588Ser | |
NM_000495.5:c.3427G>A | NP_000486.1:p.Gly1143Ser | |
NM_033380.3:c.3427G>A MANE Select | NP_203699.1:p.Gly1143Ser |