HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7526827_7526829delinsACC , CM000681.2:g.7526827_7526829delinsACC | GRCh38 |
NC_000019.9:g.7591713_7591715delinsACC , CM000681.1:g.7591713_7591715delinsACC | GRCh37 |
NC_000019.8:g.7497713_7497715delinsACC | NCBI36 |
NG_015806.1:g.9218_9220delinsACC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264079.11:c.472_474delinsACC MANE Select | ENSP00000264079.5:p.Thr158= | |
ENST00000264079.10:c.472_474delinsACC | ENSP00000264079.5:p.Thr158= | |
ENST00000394321.9:n.552_554delinsACC | ||
ENST00000596008.1:n.434_436delinsACC | ||
ENST00000598406.1:n.293_295delinsACC | ||
ENST00000601003.1:c.472_474delinsACC | ENSP00000469074.1:p.Thr158= | |
NM_020533.2:c.472_474delinsACC | NP_065394.1:p.Thr158= | |
NM_020533.3:c.472_474delinsACC MANE Select | NP_065394.1:p.Thr158= |