HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443822T>G , CM000668.2:g.32443822T>G | GRCh38 |
NC_000006.11:g.32411599T>G , CM000668.1:g.32411599T>G | GRCh37 |
NC_000006.10:g.32519577T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.677T>G MANE Select | ENSP00000378786.2:p.Val226Gly | |
ENST00000374982.5:c.602T>G | ENSP00000364121.5:p.Val201Gly | |
ENST00000395388.6:c.677T>G | ENSP00000378786.2:p.Val226Gly | |
NM_019111.4:c.677T>G | NP_061984.2:p.Val226Gly | |
NM_019111.5:c.677T>G MANE Select | NP_061984.2:p.Val226Gly |