HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31519802G= , CM000680.2:g.31519802G= | GRCh38 |
NC_000018.9:g.29099765G= , CM000680.1:g.29099765G= | GRCh37 |
NC_000018.8:g.27353763G= | NCBI36 |
NG_007072.3:g.26561G= , LRG_397:g.26561G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000682241.2:c.82-1G= | ENSP00000507600.2:n.82-1G= | |
ENST00000683654.1:c.82-1G= | ENSP00000506971.1:n.82-1G= | |
ENST00000261590.13:c.82-1G= MANE Select | ENSP00000261590.8:n.82-1G= | |
ENST00000261590.12:c.82-1G= | ENSP00000261590.8:n.82-1G= | |
ENST00000585206.1:c.82-1G= | ENSP00000462503.1:n.82-1G= | |
NM_001943.3:c.82-1G= , LRG_397t1:c.82-1G= | NP_001934.2:n.82-1G= | |
NM_001943.4:c.82-1G= | NP_001934.2:n.82-1G= | |
XM_024451095.1:c.-453-1G= | XP_024306863.1:n.-453-1G= | |
NM_001943.5:c.82-1G= MANE Select | NP_001934.2:n.82-1G= |