HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443762A>G , CM000668.2:g.32443762A>G | GRCh38 |
NC_000006.11:g.32411539A>G , CM000668.1:g.32411539A>G | GRCh37 |
NC_000006.10:g.32519517A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.617A>G MANE Select | ENSP00000378786.2:p.Asp206Gly | |
ENST00000374982.5:c.542A>G | ENSP00000364121.5:p.Asp181Gly | |
ENST00000395388.6:c.617A>G | ENSP00000378786.2:p.Asp206Gly | |
NM_019111.4:c.617A>G | NP_061984.2:p.Asp206Gly | |
NM_019111.5:c.617A>G MANE Select | NP_061984.2:p.Asp206Gly |