HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75003278A>G , CM000676.2:g.75003278A>G | GRCh38 |
NC_000014.8:g.75469981A>G , CM000676.1:g.75469981A>G | GRCh37 |
NC_000014.7:g.74539734A>G | NCBI36 |
NG_013333.1:g.5370A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266126.10:c.167A>G MANE Select | ENSP00000266126.5:p.Glu56Gly | |
ENST00000266126.9:c.167A>G | ENSP00000266126.5:p.Glu56Gly | |
ENST00000553401.5:c.140A>G | ENSP00000451681.1:p.Glu47Gly | |
ENST00000553539.1:n.307A>G | ||
ENST00000555522.1:n.225A>G | ||
ENST00000556028.5:c.167A>G | ENSP00000452311.1:p.Glu56Gly | |
NM_014239.3:c.167A>G | NP_055054.1:p.Glu56Gly | |
NM_014239.4:c.167A>G MANE Select | NP_055054.1:p.Glu56Gly |