HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154992936C= , CM000685.2:g.154992936C= | GRCh38 |
NC_000023.10:g.154221211C= , CM000685.1:g.154221211C= | GRCh37 |
NC_000023.9:g.153874405C= | NCBI36 |
NG_011403.1:g.34788G= | |
NG_011403.2:g.34788G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.601G= MANE Select | ENSP00000353393.4:p.Gly201= | |
ENST00000647125.1:c.*387G= | ENSP00000496062.1:n.*387G= | |
ENST00000360256.8:c.601G= | ENSP00000353393.4:p.Gly201= | |
ENST00000423959.5:c.496G= | ENSP00000409446.1:p.Gly166= | |
NM_000132.3:c.601G= | NP_000123.1:p.Gly201= | |
XM_011531126.1:c.496G= | XP_011529428.1:p.Gly166= | |
NM_000132.4:c.601G= MANE Select | NP_000123.1:p.Gly201= |