HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115033411C>G , CM000663.2:g.115033411C>G | GRCh38 |
NC_000001.10:g.115576032C>G , CM000663.1:g.115576032C>G | GRCh37 |
NC_000001.9:g.115377555C>G | NCBI36 |
NG_015891.1:g.8618C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256592.3:c.49C>G MANE Select | ENSP00000256592.1:p.Gln17Glu | |
ENST00000256592.2:c.49C>G | ENSP00000256592.1:p.Gln17Glu | |
ENST00000369517.1:c.49C>G | ENSP00000358530.1:p.Gln17Glu | |
NM_000549.4:c.49C>G | NP_000540.2:p.Gln17Glu | |
XM_011542065.1:c.49C>G | XP_011540367.1:p.Gln17Glu | |
XM_011542065.2:c.49C>G | XP_011540367.1:p.Gln17Glu | |
NM_000549.5:c.49C>G MANE Select | NP_000540.2:p.Gln17Glu |