HGVS | Genome Assembly |
---|---|
NC_000006.12:g.121447342T>C , CM000668.2:g.121447342T>C | GRCh38 |
NC_000006.11:g.121768488T>C , CM000668.1:g.121768488T>C | GRCh37 |
NC_000006.10:g.121810187T>C | NCBI36 |
NG_008308.1:g.16744T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000282561.4:c.495T>C MANE Select | ENSP00000282561.3:p.Phe165= | |
ENST00000647564.1:c.495T>C | ENSP00000497565.1:p.Phe165= | |
ENST00000649003.1:c.495T>C | ENSP00000497283.1:p.Phe165= | |
ENST00000650427.1:c.495T>C | ENSP00000497367.1:p.Phe165= | |
ENST00000282561.3:c.495T>C | ENSP00000282561.3:p.Phe165= | |
NM_000165.4:c.495T>C | NP_000156.1:p.Phe165= | |
NM_000165.5:c.495T>C MANE Select | NP_000156.1:p.Phe165= |