HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70175547A>T , CM000679.2:g.70175547A>T | GRCh38 |
NC_000017.10:g.68171688A>T , CM000679.1:g.68171688A>T | GRCh37 |
NC_000017.9:g.65683283A>T | NCBI36 |
NG_008798.1:g.11013A>T , LRG_328:g.11013A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.508A>T MANE Select | ENSP00000243457.2:p.Ile170Phe | |
ENST00000243457.3:c.508A>T | ENSP00000243457.2:p.Ile170Phe | |
ENST00000535240.1:c.508A>T | ENSP00000441848.1:p.Ile170Phe | |
NM_000891.2:c.508A>T , LRG_328t1:c.508A>T | NP_000882.1:p.Ile170Phe | |
XM_011524779.1:c.508A>T | XP_011523081.1:p.Ile170Phe | |
NM_000891.3:c.508A>T MANE Select | NP_000882.1:p.Ile170Phe |