HGVS | Genome Assembly |
---|---|
NC_000022.11:g.30605835A= , CM000684.2:g.30605835A= | GRCh38 |
NC_000022.10:g.31001822A= , CM000684.1:g.31001822A= | GRCh37 |
NC_000022.9:g.29331822A= | NCBI36 |
NG_007263.1:g.3662A= , LRG_116:g.3662A= |
HGVS | Amino-acid Change |
---|---|
NM_001282327.1:c.-717-318T= | NP_001269256.1:n.-717-318T= |
NM_001282328.1:c.-764-318T= | NP_001269257.1:n.-764-318T= |
ENST00000402281.5:c.-717-318T= | ENSP00000384366.1:n.-717-318T= |
ENST00000405677.5:c.-764-318T= | ENSP00000385654.1:n.-764-318T= |
ENST00000467368.1:n.62-318T= | |
ENST00000492986.1:n.251-318T= |