HGVS | Genome Assembly |
---|---|
NC_000016.10:g.56609465A= , CM000678.2:g.56609465A= | GRCh38 |
NC_000016.9:g.56643377A= , CM000678.1:g.56643377A= | GRCh37 |
NC_000016.8:g.55200878A= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000245185.6:c.*111A= MANE Select | ENSP00000245185.5:n.*111A= | |
ENST00000245185.5:c.*111A= | ENSP00000245185.5:n.*111A= | |
ENST00000561491.1:c.*280A= | ENSP00000456804.1:n.*280A= | |
ENST00000562017.1:n.871A= | ||
ENST00000563985.1:n.677A= | ||
ENST00000567300.1:n.384A= | ||
NM_005953.3:c.*111A= | NP_005944.1:n.*111A= | |
XR_933616.1:n.1025T= | ||
NM_005953.4:c.*111A= | NP_005944.1:n.*111A= | |
NM_005953.5:c.*111A= MANE Select | NP_005944.1:n.*111A= |