HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40285388C= , CM000681.2:g.40285388C= | GRCh38 |
NC_000019.9:g.40791295C= , CM000681.1:g.40791295C= | GRCh37 |
NC_000019.8:g.45483135C= | NCBI36 |
NG_012038.2:g.4971G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000392038.6:c.-292G= | ENSP00000375892.2:n.-292G= | |
ENST00000424901.5:c.-292G= | ENSP00000399532.2:n.-292G= | |
ENST00000578123.5:c.-85+60G= | ENSP00000462022.1:n.-85+60G= | |
NM_001243027.2:c.-441G= | NP_001229956.1:n.-441G= | |
NM_001243028.2:c.-348G= | NP_001229957.1:n.-348G= | |
NM_001626.5:c.-292G= | NP_001617.1:n.-292G= | |
XM_011526620.1:c.-85+60G= | XP_011524922.1:n.-85+60G= |