HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884715A>T , CM000680.2:g.13884715A>T | GRCh38 |
NC_000018.9:g.13884714A>T , CM000680.1:g.13884714A>T | GRCh37 |
NC_000018.8:g.13874714A>T | NCBI36 |
NG_011819.1:g.35822T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327606.4:c.804T>A MANE Select | ENSP00000333821.2:p.Asn268Lys | |
ENST00000327606.3:c.804T>A | ENSP00000333821.2:p.Asn268Lys | |
NM_000529.2:c.804T>A MANE Select | NP_000520.1:p.Asn268Lys | |
NM_001291911.1:c.804T>A | NP_001278840.1:p.Asn268Lys | |
XM_017025781.1:c.804T>A | XP_016881270.1:p.Asn268Lys |