HGVS | Genome Assembly |
---|---|
NC_000010.11:g.17129803C= , CM000672.2:g.17129803C= | GRCh38 |
NC_000010.10:g.17171802C= , CM000672.1:g.17171802C= | GRCh37 |
NC_000010.9:g.17211808C= | NCBI36 |
NG_008967.1:g.5015G= , LRG_540:g.5015G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377833.10:c.-38G= MANE Select | ENSP00000367064.4:n.-38G= | |
ENST00000377823.1:c.-38G= | ENSP00000367054.1:n.-38G= | |
ENST00000377833.8:c.-38G= | ENSP00000367064.4:n.-38G= | |
NM_001081.3:c.-38G= , LRG_540t1:c.-38G= | NP_001072.2:n.-38G= | |
XM_011519708.1:c.-38G= | XP_011518010.1:n.-38G= | |
XM_011519708.2:c.-38G= | XP_011518010.1:n.-38G= | |
NM_001081.4:c.-38G= MANE Select | NP_001072.2:n.-38G= |