HGVS | Genome Assembly |
---|---|
NC_000001.11:g.159302381A>G , CM000663.2:g.159302381A>G | GRCh38 |
NC_000001.10:g.159272171A>G , CM000663.1:g.159272171A>G | GRCh37 |
NC_000001.9:g.157538795A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000693622.1:c.17A>G MANE Select | ENSP00000509626.1:p.Glu6Gly | |
ENST00000368114.1:c.17A>G | ENSP00000357096.1:p.Glu6Gly | |
ENST00000368115.5:c.17A>G | ENSP00000357097.1:p.Glu6Gly | |
NM_002001.3:c.17A>G | NP_001992.1:p.Glu6Gly | |
NM_001387280.1:c.17A>G MANE Select | NP_001374209.1:p.Glu6Gly | |
NM_001387281.1:c.17A>G | NP_001374210.1:p.Glu6Gly | |
NM_001387282.1:c.17A>G | NP_001374211.1:p.Glu6Gly | |
NM_002001.4:c.17A>G | NP_001992.1:p.Glu6Gly |