HGVS | Genome Assembly |
---|---|
NC_000006.12:g.149287661T= , CM000668.2:g.149287661T= | GRCh38 |
NC_000006.11:g.149608797T= , CM000668.1:g.149608797T= | GRCh37 |
NC_000006.10:g.149650490T= | NCBI36 |
NG_021386.2:g.74738T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000606202.1:c.-121+68885T= | ENSP00000476139.1:n.-121+68885T= | |
NM_001292035.2:c.6+68885T= | NP_001278964.1:n.6+68885T= | |
NM_001292035.3:c.6+68885T= | NP_001278964.1:n.6+68885T= |