HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35500005A= , CM000668.2:g.35500005A= | GRCh38 |
NC_000006.11:g.35467782A= , CM000668.1:g.35467782A= | GRCh37 |
NC_000006.10:g.35575760A= | NCBI36 |
NG_009077.1:g.17866T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000229771.11:c.1471T= MANE Select | ENSP00000229771.6:p.Phe491= | |
ENST00000229771.10:c.1471T= | ENSP00000229771.6:p.Phe491= | |
ENST00000322263.8:c.1312T= | ENSP00000319414.4:p.Phe438= | |
ENST00000614066.4:c.1465T= | ENSP00000477534.1:p.Phe489= | |
NM_001289395.1:c.1312T= | NP_001276324.1:p.Phe438= | |
NM_003322.4:c.1471T= | NP_003313.3:p.Phe491= | |
NM_003322.5:c.1471T= | NP_003313.3:p.Phe491= | |
NM_003322.6:c.1471T= MANE Select | NP_003313.3:p.Phe491= | |
NM_001289395.2:c.1312T= | NP_001276324.1:p.Phe438= |