HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443358C>G , CM000668.2:g.32443358C>G | GRCh38 |
NC_000006.11:g.32411135C>G , CM000668.1:g.32411135C>G | GRCh37 |
NC_000006.10:g.32519113C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.502C>G MANE Select | ENSP00000378786.2:p.His168Asp | |
ENST00000374982.5:c.427C>G | ENSP00000364121.5:p.His143Asp | |
ENST00000395388.6:c.502C>G | ENSP00000378786.2:p.His168Asp | |
NM_019111.4:c.502C>G | NP_061984.2:p.His168Asp | |
NM_019111.5:c.502C>G MANE Select | NP_061984.2:p.His168Asp |