HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196996126A>T , CM000663.2:g.196996126A>T | GRCh38 |
NC_000001.10:g.196965256A>T , CM000663.1:g.196965256A>T | GRCh37 |
NC_000001.9:g.195231879A>T | NCBI36 |
NG_016365.1:g.23590A>T , LRG_227:g.23590A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.640A>T | ENSP00000514393.1:p.Asn214Tyr | |
ENST00000699467.1:n.964A>T | ||
ENST00000699468.1:c.-12A>T | ENSP00000514394.1:n.-12A>T | |
ENST00000256785.5:c.895A>T MANE Select | ENSP00000256785.4:p.Asn299Tyr | |
ENST00000256785.4:c.895A>T | ENSP00000256785.4:p.Asn299Tyr | |
NM_030787.3:c.895A>T , LRG_227t1:c.895A>T | NP_110414.1:p.Asn299Tyr | |
XM_011510020.1:c.904A>T | XP_011508322.1:p.Asn302Tyr | |
XM_011510020.2:c.904A>T | XP_011508322.1:p.Asn302Tyr | |
NM_030787.4:c.895A>T MANE Select | NP_110414.1:p.Asn299Tyr |