HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19951827A>G , CM000670.2:g.19951827A>G | GRCh38 |
NC_000008.10:g.19809338A>G , CM000670.1:g.19809338A>G | GRCh37 |
NC_000008.9:g.19853618A>G | NCBI36 |
NG_008855.1:g.17757A>G | |
NG_008855.2:g.55111A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.308A>G MANE Select | ENSP00000497642.1:p.Glu103Gly | |
ENST00000311322.8:c.308A>G | ENSP00000309757.6:p.Glu103Gly | |
ENST00000520959.5:c.80A>G | ENSP00000428496.1:p.Glu27Gly | |
ENST00000521994.1:n.565A>G | ||
ENST00000522701.5:c.308A>G | ENSP00000428557.1:p.Glu103Gly | |
ENST00000524029.5:c.308A>G | ENSP00000428237.1:p.Glu103Gly | |
NM_000237.2:c.308A>G | NP_000228.1:p.Glu103Gly | |
NM_000237.3:c.308A>G MANE Select | NP_000228.1:p.Glu103Gly |