HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443770A>G , CM000668.2:g.32443770A>G | GRCh38 |
NC_000006.11:g.32411547A>G , CM000668.1:g.32411547A>G | GRCh37 |
NC_000006.10:g.32519525A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000395388.7:c.625A>G MANE Select | ENSP00000378786.2:p.Ser209Gly | |
ENST00000374982.5:c.550A>G | ENSP00000364121.5:p.Ser184Gly | |
ENST00000395388.6:c.625A>G | ENSP00000378786.2:p.Ser209Gly | |
NM_019111.4:c.625A>G | NP_061984.2:p.Ser209Gly | |
NM_019111.5:c.625A>G MANE Select | NP_061984.2:p.Ser209Gly |