HGVS | Genome Assembly |
---|---|
NC_000018.10:g.77268500G>T , CM000680.2:g.77268500G>T | GRCh38 |
NC_000018.9:g.74980456G>T , CM000680.1:g.74980456G>T | GRCh37 |
NC_000018.8:g.73109444G>T | NCBI36 |
NG_009223.1:g.23449G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299727.5:c.733-85G>T MANE Select | ENSP00000299727.3:n.733-85G>T | |
ENST00000299727.4:c.733-85G>T | ENSP00000299727.3:n.733-85G>T | |
NM_001480.3:c.733-85G>T | NP_001471.2:n.733-85G>T | |
NM_001480.4:c.733-85G>T MANE Select | NP_001471.2:n.733-85G>T |