HGVS | Genome Assembly |
---|---|
NC_000002.12:g.232541475C>T , CM000664.2:g.232541475C>T | GRCh38 |
NC_000002.11:g.233406185C>T , CM000664.1:g.233406185C>T | GRCh37 |
NC_000002.10:g.233114429C>T | NCBI36 |
NG_012954.1:g.6749C>T | |
NG_012954.2:g.6784C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651502.1:c.452C>T MANE Select | ENSP00000498757.1:p.Ser151Phe | |
ENST00000389492.3:c.350+764C>T | ENSP00000374143.3:n.350+764C>T | |
ENST00000389494.7:c.452C>T | ENSP00000374145.3:p.Ser151Phe | |
ENST00000485094.1:n.473C>T | ||
NM_005199.4:c.452C>T | NP_005190.4:p.Ser151Phe | |
NM_005199.5:c.452C>T MANE Select | NP_005190.4:p.Ser151Phe |