HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68646945C>A , CM000666.2:g.68646945C>A | GRCh38 |
NC_000004.11:g.69512663C>A , CM000666.1:g.69512663C>A | GRCh37 |
NC_000004.10:g.69195258C>A | NCBI36 |
NG_052676.1:g.28832G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.*159G>T MANE Select | ENSP00000341045.5:n.*159G>T | |
ENST00000338206.5:c.*159G>T | ENSP00000341045.5:n.*159G>T | |
ENST00000616841.4:c.1732+20G>T | ENSP00000482004.1:n.1732+20G>T | |
NM_001076.3:c.*159G>T | NP_001067.2:n.*159G>T | |
NM_001076.4:c.*159G>T MANE Select | NP_001067.2:n.*159G>T |