HGVS | Genome Assembly |
---|---|
NC_000015.10:g.64162889G>C , CM000677.2:g.64162889G>C | GRCh38 |
NC_000015.9:g.64455088G>C , CM000677.1:g.64455088G>C | GRCh37 |
NC_000015.8:g.62242141G>C | NCBI36 |
NG_012979.1:g.5267C>G , LRG_10:g.5267C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000300026.4:c.98C>G MANE Select | ENSP00000300026.4:p.Ala33Gly | |
ENST00000561048.2:n.131C>G | ||
ENST00000680158.1:c.98C>G | ENSP00000504873.1:p.Ala33Gly | |
ENST00000681397.1:c.98C>G | ENSP00000506584.1:p.Ala33Gly | |
ENST00000681658.1:c.30+68C>G | ENSP00000505431.1:n.30+68C>G | |
ENST00000300026.3:c.98C>G | ENSP00000300026.3:p.Ala33Gly | |
ENST00000558492.1:n.118C>G | ||
ENST00000561048.1:n.133C>G | ||
NM_000942.4:c.98C>G , LRG_10t1:c.98C>G | NP_000933.1:p.Ala33Gly | |
NM_000942.5:c.98C>G MANE Select | NP_000933.1:p.Ala33Gly |