HGVS | Genome Assembly |
---|---|
NC_000016.10:g.56609263G>T , CM000678.2:g.56609263G>T | GRCh38 |
NC_000016.9:g.56643175G>T , CM000678.1:g.56643175G>T | GRCh37 |
NC_000016.8:g.55200676G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000245185.6:c.95G>T MANE Select | ENSP00000245185.5:p.Ser32Ile | |
ENST00000245185.5:c.95G>T | ENSP00000245185.5:p.Ser32Ile | |
ENST00000561491.1:c.*78G>T | ENSP00000456804.1:n.*78G>T | |
ENST00000562017.1:n.669G>T | ||
ENST00000563985.1:n.475G>T | ||
ENST00000567300.1:n.182G>T | ||
NM_005953.3:c.95G>T | NP_005944.1:p.Ser32Ile | |
NM_005953.4:c.95G>T | NP_005944.1:p.Ser32Ile | |
NM_005953.5:c.95G>T MANE Select | NP_005944.1:p.Ser32Ile |