HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67940484G= , CM000678.2:g.67940484G= | GRCh38 |
NC_000016.9:g.67974387G= , CM000678.1:g.67974387G= | GRCh37 |
NC_000016.8:g.66531888G= | NCBI36 |
NG_009778.1:g.8629C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264005.10:c.749-6C= MANE Select | ENSP00000264005.5:n.749-6C= | |
ENST00000264005.9:c.749-6C= | ENSP00000264005.5:n.749-6C= | |
ENST00000570369.5:c.156-410C= | ||
ENST00000570980.1:c.533-6C= | ENSP00000464651.1:n.533-6C= | |
ENST00000573538.5:c.487-6C= | ENSP00000463220.1:n.487-6C= | |
NM_000229.1:c.749-6C= | NP_000220.1:n.749-6C= | |
NM_000229.2:c.749-6C= MANE Select | NP_000220.1:n.749-6C= |