HGVS | Genome Assembly |
---|---|
NC_000005.10:g.150848239C>G , CM000667.2:g.150848239C>G | GRCh38 |
NC_000005.9:g.150227801C>G , CM000667.1:g.150227801C>G | GRCh37 |
NC_000005.8:g.150207994C>G | NCBI36 |
NG_027809.1:g.6717C>G | |
NG_027809.2:g.6717C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000522154.2:c.116C>G MANE Select | ENSP00000428220.1:p.Ala39Gly | |
ENST00000522154.1:c.116C>G | ENSP00000428220.1:p.Ala39Gly | |
NM_001145805.1:c.116C>G | NP_001139277.1:p.Ala39Gly | |
XM_011537641.1:c.116C>G | XP_011535943.1:p.Ala39Gly | |
NM_001346557.1:c.116C>G | NP_001333486.1:p.Ala39Gly | |
NM_001346557.2:c.116C>G | NP_001333486.1:p.Ala39Gly | |
NM_001145805.2:c.116C>G MANE Select | NP_001139277.1:p.Ala39Gly | |
NR_170598.1:n.1231C>G |