HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2171811C= , CM000673.2:g.2171811C= | GRCh38 |
NC_000011.9:g.2193041C= , CM000673.1:g.2193041C= | GRCh37 |
NC_000011.8:g.2149617C= | NCBI36 |
NG_008128.1:g.4995G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000352909.8:c.-25G= MANE Select | ENSP00000325951.4:n.-25G= | |
ENST00000352909.7:c.-25G= | ENSP00000325951.3:n.-25G= | |
XM_011520335.1:c.-25G= | XP_011518637.1:n.-25G= | |
XM_011520335.2:c.-25G= | XP_011518637.1:n.-25G= | |
NM_000360.4:c.-25G= MANE Select | NP_000351.2:n.-25G= | |
NM_199292.3:c.-25G= | NP_954986.2:n.-25G= | |
NM_199293.3:c.-25G= | NP_954987.2:n.-25G= |