HGVS | Genome Assembly |
---|---|
NC_000011.10:g.70206171G>T , CM000673.2:g.70206171G>T | GRCh38 |
NC_000011.9:g.70052277G>T , CM000673.1:g.70052277G>T | GRCh37 |
NC_000011.8:g.69729925G>T | NCBI36 |
NG_027966.1:g.8009G>T , LRG_228:g.8009G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301838.5:c.325G>T MANE Select | ENSP00000301838.5:p.Gly109Trp | |
ENST00000301838.4:c.325G>T | ENSP00000301838.4:p.Gly109Trp | |
NM_003824.3:c.325G>T , LRG_228t1:c.325G>T | NP_003815.1:p.Gly109Trp | |
NM_003824.4:c.325G>T MANE Select | NP_003815.1:p.Gly109Trp |