HGVS | Genome Assembly |
---|---|
NC_000005.10:g.150848262T>G , CM000667.2:g.150848262T>G | GRCh38 |
NC_000005.9:g.150227824T>G , CM000667.1:g.150227824T>G | GRCh37 |
NC_000005.8:g.150208017T>G | NCBI36 |
NG_027809.1:g.6740T>G | |
NG_027809.2:g.6740T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000522154.2:c.139T>G MANE Select | ENSP00000428220.1:p.Ser47Ala | |
ENST00000522154.1:c.139T>G | ENSP00000428220.1:p.Ser47Ala | |
NM_001145805.1:c.139T>G | NP_001139277.1:p.Ser47Ala | |
XM_011537641.1:c.139T>G | XP_011535943.1:p.Ser47Ala | |
NM_001346557.1:c.139T>G | NP_001333486.1:p.Ser47Ala | |
NM_001346557.2:c.139T>G | NP_001333486.1:p.Ser47Ala | |
NM_001145805.2:c.139T>G MANE Select | NP_001139277.1:p.Ser47Ala | |
NR_170598.1:n.1254T>G |