HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29070988G= , CM000664.2:g.29070988G= | GRCh38 |
NC_000002.11:g.29293854G= , CM000664.1:g.29293854G= | GRCh37 |
NC_000002.10:g.29147358G= | NCBI36 |
NG_021427.1:g.8274C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3274C= MANE Select | ENSP00000332809.4:p.Pro1092= | |
ENST00000331664.5:c.3274C= | ENSP00000332809.4:p.Pro1092= | |
NM_001029883.2:c.3274C= | NP_001025054.1:p.Pro1092= | |
XM_011532826.1:c.3274C= | XP_011531128.1:p.Pro1092= | |
XR_939901.1:n.185+1821G= | ||
XR_939902.1:n.173+1833G= | ||
NM_001029883.3:c.3274C= MANE Select | NP_001025054.1:p.Pro1092= |