HGVS | Genome Assembly |
---|---|
NC_000020.11:g.6778390T= , CM000682.2:g.6778390T= | GRCh38 |
NC_000020.10:g.6759037T= , CM000682.1:g.6759037T= | GRCh37 |
NC_000020.9:g.6707037T= | NCBI36 |
NG_023233.1:g.15293T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378827.5:c.492T= MANE Select | ENSP00000368104.3:p.Asn164= | |
ENST00000378827.4:c.492T= | ENSP00000368104.3:p.Asn164= | |
NM_001200.2:c.492T= | NP_001191.1:p.Asn164= | |
XM_011529323.1:c.24T= | XP_011527625.1:p.Asn8= | |
NM_001200.3:c.492T= | NP_001191.1:p.Asn164= | |
NM_001200.4:c.492T= MANE Select | NP_001191.1:p.Asn164= |