HGVS | Genome Assembly |
---|---|
NC_000002.12:g.219060569C= , CM000664.2:g.219060569C= | GRCh38 |
NC_000002.11:g.219925291C= , CM000664.1:g.219925291C= | GRCh37 |
NC_000002.10:g.219633535C= | NCBI36 |
NG_016741.1:g.4948G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295731.7:c.-102G= MANE Select | ENSP00000295731.5:n.-102G= | |
NM_002181.4:c.-102G= MANE Select | NP_002172.2:n.-102G= |