HGVS | Genome Assembly |
---|---|
NC_000004.12:g.70642693A>T , CM000666.2:g.70642693A>T | GRCh38 |
NC_000004.11:g.71508410A>T , CM000666.1:g.71508410A>T | GRCh37 |
NC_000004.10:g.71727274A>T | NCBI36 |
NG_013024.1:g.18950A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000396073.4:c.1267A>T MANE Select | ENSP00000379383.4:p.Lys423Ter | |
ENST00000396073.3:c.1267A>T | ENSP00000379383.3:p.Lys423Ter | |
ENST00000472903.5:n.99+4850A>T | ||
NM_031889.2:c.1267A>T | NP_114095.2:p.Lys423Ter | |
XM_006714056.2:c.1267A>T | XP_006714119.1:p.Lys423Ter | |
XM_006714056.4:c.1267A>T | XP_006714119.1:p.Lys423Ter | |
NM_001368133.1:c.613A>T | NP_001355062.1:p.Lys205Ter | |
NM_031889.3:c.1267A>T MANE Select | NP_114095.2:p.Lys423Ter |