HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110914188T>A , CM000674.2:g.110914188T>A | GRCh38 |
NC_000012.11:g.111351992T>A , CM000674.1:g.111351992T>A | GRCh37 |
NC_000012.10:g.109836375T>A | NCBI36 |
NG_007554.1:g.11390A>T , LRG_393:g.11390A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000228841.15:c.272A>T MANE Select | ENSP00000228841.8:p.Lys91Met | |
ENST00000663220.1:c.215A>T | ENSP00000499568.1:p.Lys72Met | |
ENST00000228841.12:c.272A>T | ENSP00000228841.7:p.Lys91Met | |
ENST00000548438.1:c.230A>T | ENSP00000447154.1:p.Lys77Met | |
ENST00000549029.1:n.103A>T | ||
NM_000432.3:c.272A>T , LRG_393t1:c.272A>T | NP_000423.2:p.Lys91Met | |
NM_000432.4:c.272A>T MANE Select | NP_000423.2:p.Lys91Met |