HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31498272C>G , CM000680.2:g.31498272C>G | GRCh38 |
NC_000018.9:g.29078235C>G , CM000680.1:g.29078235C>G | GRCh37 |
NC_000018.8:g.27332233C>G | NCBI36 |
NG_007072.3:g.5031C>G , LRG_397:g.5031C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682241.2:c.21C>G | ENSP00000507600.2:p.Arg7= | |
ENST00000683654.1:c.21C>G | ENSP00000506971.1:p.Arg7= | |
ENST00000261590.13:c.21C>G MANE Select | ENSP00000261590.8:p.Arg7= | |
ENST00000261590.12:c.21C>G | ENSP00000261590.8:p.Arg7= | |
ENST00000585206.1:c.21C>G | ENSP00000462503.1:p.Arg7= | |
NM_001943.3:c.21C>G , LRG_397t1:c.21C>G | NP_001934.2:p.Arg7= | |
NM_001943.4:c.21C>G | NP_001934.2:p.Arg7= | |
NM_001943.5:c.21C>G MANE Select | NP_001934.2:p.Arg7= |