HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20188898G= , CM000675.2:g.20188898G= | GRCh38 |
NC_000013.10:g.20763037G= , CM000675.1:g.20763037G= | GRCh37 |
NC_000013.9:g.19661037G= | NCBI36 |
NG_008358.1:g.9078C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.*3C= | ENSP00000372295.1:n.*3C= | |
ENST00000382848.5:c.*3C= MANE Select | ENSP00000372299.4:n.*3C= | |
ENST00000382844.1:c.*3C= | ENSP00000372295.1:n.*3C= | |
ENST00000382848.4:c.*3C= | ENSP00000372299.4:n.*3C= | |
NM_004004.5:c.*3C= | NP_003995.2:n.*3C= | |
XM_011535049.1:c.*3C= | XP_011533351.1:n.*3C= | |
XM_011535049.2:c.*3C= | XP_011533351.1:n.*3C= | |
NM_004004.6:c.*3C= MANE Select | NP_003995.2:n.*3C= |