HGVS | Genome Assembly |
---|---|
NC_000002.12:g.208129678G>A , CM000664.2:g.208129678G>A | GRCh38 |
NC_000002.11:g.208994402G>A , CM000664.1:g.208994402G>A | GRCh37 |
NC_000002.10:g.208702647G>A | NCBI36 |
NG_008038.1:g.5153C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282141.4:c.15C>T MANE Select | ENSP00000282141.3:p.Thr5= | |
ENST00000282141.3:c.15C>T | ENSP00000282141.3:p.Thr5= | |
NM_020989.3:c.15C>T | NP_066269.1:p.Thr5= | |
NR_038437.1:n.98-7378G>A | ||
XM_011510661.1:c.15C>T | XP_011508963.1:p.Thr5= | |
XM_011510662.1:c.15C>T | XP_011508964.1:p.Thr5= | |
XM_011510663.1:c.-115C>T | XP_011508965.1:n.-115C>T | |
NM_020989.4:c.15C>T MANE Select | NP_066269.1:p.Thr5= |