HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225614A>T , CM000668.2:g.3225614A>T | GRCh38 |
NC_000006.11:g.3225848A>T , CM000668.1:g.3225848A>T | GRCh37 |
NC_000006.10:g.3170847A>T | NCBI36 |
NG_016715.1:g.7121T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.475T>A MANE Select | ENSP00000259818.6:p.Tyr159Asn | |
ENST00000680070.1:n.1405T>A | ||
ENST00000681707.1:n.1302T>A | ||
ENST00000681757.1:n.780T>A | ||
ENST00000259818.7:c.475T>A | ENSP00000259818.6:p.Tyr159Asn | |
ENST00000473006.1:n.592T>A | ||
NM_178012.4:c.475T>A | NP_821080.1:p.Tyr159Asn | |
XM_011514571.1:c.259T>A | XP_011512873.1:p.Tyr87Asn | |
NM_178012.5:c.475T>A MANE Select | NP_821080.1:p.Tyr159Asn |