HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169485626C= , CM000663.2:g.169485626C= | GRCh38 |
NC_000001.10:g.169454864C= , CM000663.1:g.169454864C= | GRCh37 |
NC_000001.9:g.167721488C= | NCBI36 |
NG_008255.1:g.5345G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000236137.10:c.141G= MANE Select | ENSP00000236137.5:p.Arg47= | |
ENST00000646596.1:c.141G= | ENSP00000494404.1:p.Arg47= | |
ENST00000236137.9:c.141G= | ENSP00000236137.5:p.Arg47= | |
ENST00000367804.4:c.141G= | ENSP00000356778.3:p.Arg47= | |
NM_006996.2:c.141G= | NP_008927.1:p.Arg47= | |
XM_011509076.1:c.12+427G= | XP_011507378.1:n.12+427G= | |
XM_011509077.1:c.141G= | XP_011507379.1:p.Arg47= | |
NM_001319667.1:c.141G= | NP_001306596.1:p.Arg47= | |
NM_006996.3:c.141G= MANE Select | NP_008927.1:p.Arg47= |