HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213527C>A , CM000667.2:g.1213527C>A | GRCh38 |
NC_000005.9:g.1213642C>A , CM000667.1:g.1213642C>A | GRCh37 |
NC_000005.8:g.1266642C>A | NCBI36 |
NG_008282.1:g.16933C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000304460.11:c.728C>A MANE Select | ENSP00000305302.10:p.Thr243Lys | |
ENST00000304460.10:c.728C>A | ENSP00000305302.10:p.Thr243Lys | |
ENST00000515652.5:c.636C>A | ENSP00000425701.1:p.Asp212Glu | |
NM_001003841.2:c.728C>A | NP_001003841.1:p.Thr243Lys | |
NM_001003841.3:c.728C>A MANE Select | NP_001003841.1:p.Thr243Lys |