HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225794T>A , CM000668.2:g.3225794T>A | GRCh38 |
NC_000006.11:g.3226028T>A , CM000668.1:g.3226028T>A | GRCh37 |
NC_000006.10:g.3171027T>A | NCBI36 |
NG_016715.1:g.6941A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.295A>T MANE Select | ENSP00000259818.6:p.Asn99Tyr | |
ENST00000680070.1:n.1225A>T | ||
ENST00000681707.1:n.1122A>T | ||
ENST00000681757.1:n.600A>T | ||
ENST00000259818.7:c.295A>T | ENSP00000259818.6:p.Asn99Tyr | |
ENST00000473006.1:n.412A>T | ||
NM_178012.4:c.295A>T | NP_821080.1:p.Asn99Tyr | |
XM_011514571.1:c.79A>T | XP_011512873.1:p.Asn27Tyr | |
NM_178012.5:c.295A>T MANE Select | NP_821080.1:p.Asn99Tyr |