HGVS | Genome Assembly |
---|---|
NC_000005.10:g.71719660C= , CM000667.2:g.71719660C= | GRCh38 |
NC_000005.9:g.71015487C= , CM000667.1:g.71015487C= | GRCh37 |
NC_000005.8:g.71051243C= | NCBI36 |
NG_015988.1:g.5498C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296777.5:c.159+208C= MANE Select | ENSP00000296777.4:n.159+208C= | |
ENST00000296777.4:c.159+208C= | ENSP00000296777.4:n.159+208C= | |
ENST00000513096.1:n.82C= | ||
NM_004291.3:c.159+208C= | NP_004282.1:n.159+208C= | |
NM_004291.4:c.159+208C= MANE Select | NP_004282.1:n.159+208C= |