HGVS | Genome Assembly |
---|---|
NC_000023.11:g.48527252C>T , CM000685.2:g.48527252C>T | GRCh38 |
NC_000023.10:g.48385640C>T , CM000685.1:g.48385640C>T | GRCh37 |
NC_000023.9:g.48270584C>T | NCBI36 |
NG_007452.1:g.10477C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000495186.6:c.436C>T MANE Select | ENSP00000417052.1:p.Leu146Phe | |
ENST00000651615.1:c.436C>T | ENSP00000498524.1:p.Leu146Phe | |
ENST00000276096.10:n.394C>T | ||
ENST00000414061.1:c.436C>T | ||
ENST00000446158.5:c.436C>T | ENSP00000390031.1:p.Leu146Phe | |
ENST00000466461.1:n.275C>T | ||
ENST00000495186.5:c.436C>T | ENSP00000417052.1:p.Leu146Phe | |
ENST00000498425.1:n.557C>T | ||
NM_006579.2:c.436C>T | NP_006570.1:p.Leu146Phe | |
NM_006579.3:c.436C>T MANE Select | NP_006570.1:p.Leu146Phe |