HGVS | Genome Assembly |
---|---|
NC_000006.12:g.160650438G>A , CM000668.2:g.160650438G>A | GRCh38 |
NC_000006.11:g.161071470G>A , CM000668.1:g.161071470G>A | GRCh37 |
NC_000006.10:g.160991460G>A | NCBI36 |
NG_016147.1:g.20938C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000316300.10:c.109C>T MANE Select | ENSP00000321334.6:p.Arg37Ter | |
ENST00000316300.9:c.109C>T | ENSP00000321334.5:p.Arg37Ter | |
NM_005577.2:c.109C>T | NP_005568.2:p.Arg37Ter | |
NM_005577.3:c.109C>T | NP_005568.2:p.Arg37Ter | |
NM_005577.4:c.109C>T MANE Select | NP_005568.2:p.Arg37Ter |