HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443299G>A , CM000668.2:g.32443299G>A | GRCh38 |
NC_000006.11:g.32411076G>A , CM000668.1:g.32411076G>A | GRCh37 |
NC_000006.10:g.32519054G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.443G>A MANE Select | ENSP00000378786.2:p.Arg148Gln | |
ENST00000374982.5:c.368G>A | ENSP00000364121.5:p.Arg123Gln | |
ENST00000395388.6:c.443G>A | ENSP00000378786.2:p.Arg148Gln | |
NM_019111.4:c.443G>A | NP_061984.2:p.Arg148Gln | |
NM_019111.5:c.443G>A MANE Select | NP_061984.2:p.Arg148Gln |