HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131877066T>A , CM000668.2:g.131877066T>A | GRCh38 |
NC_000006.11:g.132198206T>A , CM000668.1:g.132198206T>A | GRCh37 |
NC_000006.10:g.132239899T>A | NCBI36 |
NG_008206.1:g.74051T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000683687.1:n.670T>A | ||
ENST00000684536.1:n.296T>A | ||
ENST00000647893.1:c.1798T>A MANE Select | ENSP00000498074.1:p.Tyr600Asn | |
ENST00000647981.1:n.483T>A | ||
ENST00000650437.1:c.1289T>A | ||
ENST00000360971.6:c.1798T>A | ENSP00000354238.2:p.Tyr600Asn | |
ENST00000459624.1:n.842T>A | ||
ENST00000513998.5:c.*635T>A | ENSP00000422424.1:n.*635T>A | |
NM_006208.2:c.1798T>A | NP_006199.2:p.Tyr600Asn | |
XM_011535896.1:c.688T>A | XP_011534198.1:p.Tyr230Asn | |
NM_006208.3:c.1798T>A MANE Select | NP_006199.2:p.Tyr600Asn |