HGVS | Genome Assembly |
---|---|
NC_000002.12:g.219060484G= , CM000664.2:g.219060484G= | GRCh38 |
NC_000002.11:g.219925206G= , CM000664.1:g.219925206G= | GRCh37 |
NC_000002.10:g.219633450G= | NCBI36 |
NG_016741.1:g.5033C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295731.7:c.-17C= MANE Select | ENSP00000295731.5:n.-17C= | |
NM_002181.3:c.-17C= | NP_002172.2:n.-17C= | |
NM_002181.4:c.-17C= MANE Select | NP_002172.2:n.-17C= |