HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94021334T>C , CM000663.2:g.94021334T>C | GRCh38 |
NC_000001.10:g.94486890T>C , CM000663.1:g.94486890T>C | GRCh37 |
NC_000001.9:g.94259478T>C | NCBI36 |
NG_009073.1:g.104816A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4924A>G MANE Select | ENSP00000359245.3:p.Ser1642Gly | |
ENST00000370225.3:c.4924A>G | ENSP00000359245.3:p.Ser1642Gly | |
ENST00000460514.1:n.418A>G | ||
ENST00000470771.1:n.34A>G | ||
ENST00000536513.5:c.1300A>G | ENSP00000439707.2:p.Ser434Gly | |
NM_000350.2:c.4924A>G | NP_000341.2:p.Ser1642Gly | |
NM_000350.3:c.4924A>G MANE Select | NP_000341.2:p.Ser1642Gly |