HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68647116C>A , CM000666.2:g.68647116C>A | GRCh38 |
NC_000004.11:g.69512834C>A , CM000666.1:g.69512834C>A | GRCh37 |
NC_000004.10:g.69195429C>A | NCBI36 |
NG_052676.1:g.28661G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.1581G>T MANE Select | ENSP00000341045.5:p.Lys527Asn | |
ENST00000338206.5:c.1581G>T | ENSP00000341045.5:p.Lys527Asn | |
ENST00000616841.4:c.1581G>T | ENSP00000482004.1:p.Lys527Asn | |
NM_001076.3:c.1581G>T | NP_001067.2:p.Lys527Asn | |
NM_001076.4:c.1581G>T MANE Select | NP_001067.2:p.Lys527Asn |