HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29071118A>T , CM000664.2:g.29071118A>T | GRCh38 |
NC_000002.11:g.29293984A>T , CM000664.1:g.29293984A>T | GRCh37 |
NC_000002.10:g.29147488A>T | NCBI36 |
NG_021427.1:g.8144T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3144T>A MANE Select | ENSP00000332809.4:p.Thr1048= | |
ENST00000331664.5:c.3144T>A | ENSP00000332809.4:p.Thr1048= | |
NM_001029883.2:c.3144T>A | NP_001025054.1:p.Thr1048= | |
XM_011532826.1:c.3144T>A | XP_011531128.1:p.Thr1048= | |
XR_939901.1:n.185+1951A>T | ||
XR_939902.1:n.173+1963A>T | ||
NM_001029883.3:c.3144T>A MANE Select | NP_001025054.1:p.Thr1048= |