HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884853G= , CM000680.2:g.13884853G= | GRCh38 |
NC_000018.9:g.13884852G= , CM000680.1:g.13884852G= | GRCh37 |
NC_000018.8:g.13874852G= | NCBI36 |
NG_011819.1:g.35684C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327606.4:c.666C= MANE Select | ENSP00000333821.2:p.Thr222= | |
ENST00000327606.3:c.666C= | ENSP00000333821.2:p.Thr222= | |
NM_000529.2:c.666C= MANE Select | NP_000520.1:p.Thr222= | |
NM_001291911.1:c.666C= | NP_001278840.1:p.Thr222= | |
XM_017025781.1:c.666C= | XP_016881270.1:p.Thr222= |