HGVS | Genome Assembly |
---|---|
NC_000009.12:g.137199393C>A , CM000671.2:g.137199393C>A | GRCh38 |
NC_000009.11:g.140093845C>A , CM000671.1:g.140093845C>A | GRCh37 |
NC_000009.10:g.139213666C>A | NCBI36 |
NG_027801.1:g.6319G>T | |
NG_027801.2:g.9801G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409012.6:c.1319G>T MANE Select | ENSP00000387100.4:p.Gly440Val | |
ENST00000333046.8:c.713G>T | ENSP00000327617.4:p.Gly238Val | |
ENST00000409012.4:c.1319G>T | ENSP00000387100.4:p.Gly440Val | |
ENST00000541945.1:n.90+4711G>T | ||
NM_001128228.2:c.1319G>T | NP_001121700.2:p.Gly440Val | |
NM_001128228.3:c.1319G>T MANE Select | NP_001121700.2:p.Gly440Val |