HGVS | Genome Assembly |
---|---|
NC_000017.11:g.29533907A= , CM000679.2:g.29533907A= | GRCh38 |
NC_000017.10:g.27860925A= , CM000679.1:g.27860925A= | GRCh37 |
NC_000017.9:g.24885051A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261716.8:c.2362-211A= MANE Select | ENSP00000261716.3:n.2362-211A= | |
ENST00000261716.7:c.2362-211A= | ENSP00000261716.3:n.2362-211A= | |
ENST00000536202.1:c.1918-211A= | ENSP00000438819.1:n.1918-211A= | |
NM_020791.2:c.2362-211A= | NP_065842.1:n.2362-211A= | |
NM_025142.1:c.1918-211A= | NP_079418.1:n.1918-211A= | |
XM_011525060.1:c.2362-211A= | XP_011523362.1:n.2362-211A= | |
XM_011525060.2:c.2362-211A= | XP_011523362.1:n.2362-211A= | |
NM_020791.4:c.2362-211A= MANE Select | NP_065842.1:n.2362-211A= |