HGVS | Genome Assembly |
---|---|
NC_000001.11:g.155300270C>A , CM000663.2:g.155300270C>A | GRCh38 |
NC_000001.10:g.155270061C>A , CM000663.1:g.155270061C>A | GRCh37 |
NC_000001.9:g.153536685C>A | NCBI36 |
NG_011677.1:g.6165G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342741.6:c.111G>T MANE Select | ENSP00000339933.4:p.Gly37= | |
ENST00000434082.3:c.-21-61G>T | ENSP00000398037.3:n.-21-61G>T | |
ENST00000342741.4:c.111G>T | ENSP00000339933.4:p.Gly37= | |
ENST00000392414.7:c.18G>T | ENSP00000376214.3:p.Gly6= | |
ENST00000434082.2:c.77-61G>T | ENSP00000398037.2:n.77-61G>T | |
NM_000298.5:c.111G>T | NP_000289.1:p.Gly37= | |
NM_181871.3:c.18G>T | NP_870986.1:p.Gly6= | |
XM_005245266.3:c.270G>T | XP_005245323.1:p.Gly90= | |
XM_006711386.2:c.-21-61G>T | XP_006711449.1:n.-21-61G>T | |
XM_011509639.1:c.270G>T | XP_011507941.1:p.Gly90= | |
XM_011509640.1:c.-82G>T | XP_011507942.1:n.-82G>T | |
NM_000298.6:c.111G>T MANE Select | NP_000289.1:p.Gly37= | |
XM_006711386.4:c.-21-61G>T | XP_006711449.1:n.-21-61G>T | |
XM_011509640.3:c.-82G>T | XP_011507942.1:n.-82G>T | |
XM_017001493.1:c.111G>T | XP_016856982.1:p.Gly37= | |
NM_181871.4:c.18G>T | NP_870986.1:p.Gly6= |