HGVS | Genome Assembly |
---|---|
NC_000015.10:g.64162943G>C , CM000677.2:g.64162943G>C | GRCh38 |
NC_000015.9:g.64455142G>C , CM000677.1:g.64455142G>C | GRCh37 |
NC_000015.8:g.62242195G>C | NCBI36 |
NG_012979.1:g.5213C>G , LRG_10:g.5213C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000300026.4:c.44C>G MANE Select | ENSP00000300026.4:p.Ala15Gly | |
ENST00000561048.2:n.77C>G | ||
ENST00000680158.1:c.44C>G | ENSP00000504873.1:p.Ala15Gly | |
ENST00000681397.1:c.44C>G | ENSP00000506584.1:p.Ala15Gly | |
ENST00000681658.1:c.30+14C>G | ENSP00000505431.1:n.30+14C>G | |
ENST00000300026.3:c.44C>G | ENSP00000300026.3:p.Ala15Gly | |
ENST00000558492.1:n.64C>G | ||
ENST00000561048.1:n.79C>G | ||
NM_000942.4:c.44C>G , LRG_10t1:c.44C>G | NP_000933.1:p.Ala15Gly | |
NM_000942.5:c.44C>G MANE Select | NP_000933.1:p.Ala15Gly |