HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20759888T>G , CM000686.2:g.20759888T>G | GRCh38 |
NC_000024.9:g.22921774T>G , CM000686.1:g.22921774T>G | GRCh37 |
NC_000024.8:g.21331162T>G | NCBI36 |
NG_032924.1:g.8821T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000629237.2:c.102T>G MANE Select | ENSP00000486252.1:p.Gly34= | |
ENST00000629237.1:c.102T>G | ENSP00000486252.1:p.Gly34= | |
NM_001039567.2:c.102T>G | NP_001034656.1:p.Gly34= | |
XM_011531423.1:c.51T>G | XP_011529725.1:p.Gly17= | |
NM_001039567.3:c.102T>G MANE Select | NP_001034656.1:p.Gly34= |