HGVS | Genome Assembly |
---|---|
NC_000005.10:g.93585345A>G , CM000667.2:g.93585345A>G | GRCh38 |
NC_000005.9:g.92921051A>G , CM000667.1:g.92921051A>G | GRCh37 |
NC_000005.8:g.92946807A>G | NCBI36 |
NG_034119.1:g.7009A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000615873.2:c.247A>G | ENSP00000481517.1:p.Ser83Gly | |
ENST00000327111.8:c.322A>G MANE Select | ENSP00000325819.3:p.Ser108Gly | |
ENST00000647447.1:c.169A>G | ENSP00000495740.1:p.Ser57Gly | |
ENST00000327111.7:c.322A>G | ENSP00000325819.3:p.Ser108Gly | |
ENST00000615873.1:c.247A>G | ENSP00000481517.1:p.Ser83Gly | |
NM_005654.5:c.322A>G | NP_005645.1:p.Ser108Gly | |
NM_005654.6:c.322A>G MANE Select | NP_005645.1:p.Ser108Gly |