HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88720083G= , CM000678.2:g.88720083G= | GRCh38 |
NC_000016.9:g.88786491G= , CM000678.1:g.88786491G= | GRCh37 |
NC_000016.8:g.87313992G= | NCBI36 |
NG_042229.1:g.70138C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301015.14:c.6150C= MANE Select | ENSP00000301015.9:p.Pro2050= | |
ENST00000466823.3:c.176C= | ||
ENST00000301015.13:c.6150C= | ENSP00000301015.9:p.Pro2050= | |
ENST00000466823.2:c.176C= | ||
ENST00000495568.7:n.391C= | ||
ENST00000497793.2:n.305C= | ||
NM_001142864.2:c.6150C= | NP_001136336.2:p.Pro2050= | |
NM_001142864.3:c.6150C= | NP_001136336.2:p.Pro2050= | |
NM_001142864.4:c.6150C= MANE Select | NP_001136336.2:p.Pro2050= |