HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196996117A>T , CM000663.2:g.196996117A>T | GRCh38 |
NC_000001.10:g.196965247A>T , CM000663.1:g.196965247A>T | GRCh37 |
NC_000001.9:g.195231870A>T | NCBI36 |
NG_016365.1:g.23581A>T , LRG_227:g.23581A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.631A>T | ENSP00000514393.1:p.Asn211Tyr | |
ENST00000699467.1:n.955A>T | ||
ENST00000699468.1:c.-21A>T | ENSP00000514394.1:n.-21A>T | |
ENST00000256785.5:c.886A>T MANE Select | ENSP00000256785.4:p.Asn296Tyr | |
ENST00000256785.4:c.886A>T | ENSP00000256785.4:p.Asn296Tyr | |
NM_030787.3:c.886A>T , LRG_227t1:c.886A>T | NP_110414.1:p.Asn296Tyr | |
XM_011510020.1:c.895A>T | XP_011508322.1:p.Asn299Tyr | |
XM_011510020.2:c.895A>T | XP_011508322.1:p.Asn299Tyr | |
NM_030787.4:c.886A>T MANE Select | NP_110414.1:p.Asn296Tyr |