HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43169199T>A , CM000683.2:g.43169199T>A | GRCh38 |
NG_009823.1:g.5169T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291554.6:c.100T>A MANE Select | ENSP00000291554.2:p.Tyr34Asn | |
ENST00000482775.1:n.113T>A | ||
NM_000394.3:c.100T>A | NP_000385.1:p.Tyr34Asn | |
XR_001755073.1:n.647+1838A>T | ||
NM_000394.4:c.100T>A MANE Select | NP_000385.1:p.Tyr34Asn |