HGVS | Genome Assembly |
---|---|
NC_000008.11:g.98158229C>G , CM000670.2:g.98158229C>G | GRCh38 |
NC_000008.10:g.99170457C>G , CM000670.1:g.99170457C>G | GRCh37 |
NC_000008.9:g.99239633C>G | NCBI36 |
NG_052869.1:g.45937C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000401707.7:c.3033C>G MANE Select | ENSP00000385787.2:p.Ala1011= | |
ENST00000349693.3:c.3033C>G | ENSP00000339529.3:p.Ala1011= | |
ENST00000401707.6:c.3033C>G | ENSP00000385787.2:p.Ala1011= | |
NM_001145860.1:c.3033C>G | NP_001139332.1:p.Ala1011= | |
NM_001145861.1:c.3033C>G | NP_001139333.1:p.Ala1011= | |
NM_015029.2:c.3033C>G | NP_055844.2:p.Ala1011= | |
NM_001145860.2:c.3033C>G MANE Select | NP_001139332.1:p.Ala1011= | |
NM_001145861.2:c.3033C>G | NP_001139333.1:p.Ala1011= | |
NM_015029.3:c.3033C>G | NP_055844.2:p.Ala1011= |