HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20189758C= , CM000675.2:g.20189758C= | GRCh38 |
NC_000013.10:g.20763897C= , CM000675.1:g.20763897C= | GRCh37 |
NC_000013.9:g.19661897C= | NCBI36 |
NG_008358.1:g.8218G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.-177G= | ENSP00000372295.1:n.-177G= | |
ENST00000382848.5:c.-22-155G= MANE Select | ENSP00000372299.4:n.-22-155G= | |
ENST00000382844.1:c.-177G= | ENSP00000372295.1:n.-177G= | |
ENST00000382848.4:c.-22-155G= | ENSP00000372299.4:n.-22-155G= | |
NM_004004.5:c.-22-155G= | NP_003995.2:n.-22-155G= | |
XM_011535049.1:c.-22-155G= | XP_011533351.1:n.-22-155G= | |
XM_011535049.2:c.-22-155G= | XP_011533351.1:n.-22-155G= | |
NM_004004.6:c.-22-155G= MANE Select | NP_003995.2:n.-22-155G= |