HGVS | Genome Assembly |
---|---|
NC_000014.9:g.50153065T= , CM000676.2:g.50153065T= | GRCh38 |
NC_000014.8:g.50619783T= , CM000676.1:g.50619783T= | GRCh37 |
NC_000014.7:g.49689533T= | NCBI36 |
NG_051073.1:g.83629A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216373.10:c.2161+5A= MANE Select | ENSP00000216373.5:n.2161+5A= | |
ENST00000216373.9:c.2161+5A= | ENSP00000216373.5:n.2161+5A= | |
ENST00000543680.5:c.2062+5A= | ENSP00000445328.1:n.2062+5A= | |
NM_006939.2:c.2161+5A= | NP_008870.2:n.2161+5A= | |
XM_005268021.1:c.1981+5A= | XP_005268078.1:n.1981+5A= | |
XM_011537103.1:c.2122+5A= | XP_011535405.1:n.2122+5A= | |
XM_011537104.1:c.2161+5A= | XP_011535406.1:n.2161+5A= | |
NM_006939.3:c.2161+5A= | NP_008870.2:n.2161+5A= | |
NM_006939.4:c.2161+5A= MANE Select | NP_008870.2:n.2161+5A= |