HGVS | Genome Assembly |
---|---|
NC_000001.11:g.147908289G>T , CM000663.2:g.147908289G>T | GRCh38 |
NC_000001.10:g.147380416G>T , CM000663.1:g.147380416G>T | GRCh37 |
NC_000001.9:g.145847040G>T | NCBI36 |
NG_016242.1:g.10471G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369235.2:c.334G>T MANE Select | ENSP00000358238.1:p.Glu112Ter | |
ENST00000369235.1:c.334G>T | ENSP00000358238.1:p.Glu112Ter | |
NM_005267.4:c.334G>T | NP_005258.2:p.Glu112Ter | |
XM_011509416.1:c.334G>T | XP_011507718.1:p.Glu112Ter | |
XM_011509417.1:c.334G>T | XP_011507719.1:p.Glu112Ter | |
XM_011509417.2:c.334G>T | XP_011507719.1:p.Glu112Ter | |
XR_002956281.1:n.1249G>T | ||
NM_005267.5:c.334G>T MANE Select | NP_005258.2:p.Glu112Ter |