HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23200720A>C , CM000670.2:g.23200720A>C | GRCh38 |
NC_000008.10:g.23058233A>C , CM000670.1:g.23058233A>C | GRCh37 |
NC_000008.9:g.23114178A>C | NCBI36 |
NG_032107.1:g.29448T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000221132.8:c.670T>G MANE Select | ENSP00000221132.3:p.Trp224Gly | |
ENST00000221132.7:c.670T>G | ENSP00000221132.3:p.Trp224Gly | |
ENST00000524158.5:c.64T>G | ENSP00000428884.1:p.Trp22Gly | |
ENST00000613472.1:c.196T>G | ENSP00000480778.1:p.Trp66Gly | |
NM_003844.3:c.670T>G | NP_003835.3:p.Trp224Gly | |
NM_003844.4:c.670T>G MANE Select | NP_003835.3:p.Trp224Gly |