HGVS | Genome Assembly |
---|---|
NC_000019.10:g.17816956A>C , CM000681.2:g.17816956A>C | GRCh38 |
NC_000019.9:g.17927765A>C , CM000681.1:g.17927765A>C | GRCh37 |
NC_000019.8:g.17788765A>C | NCBI36 |
NG_012092.1:g.9556T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000317306.8:c.294T>G MANE Select | ENSP00000321724.6:p.Ser98= | |
ENST00000317306.7:c.294T>G | ENSP00000321724.6:p.Ser98= | |
ENST00000379695.5:c.389T>G | ENSP00000369017.4:p.Leu130Arg | |
ENST00000598577.1:c.315T>G | ||
NM_001265587.1:c.389T>G | NP_001252516.1:p.Leu130Arg | |
NM_005543.3:c.294T>G | NP_005534.2:p.Ser98= | |
NM_001265587.2:c.389T>G | NP_001252516.1:p.Leu130Arg | |
NM_005543.4:c.294T>G MANE Select | NP_005534.2:p.Ser98= |