HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226640_5226641delinsGC , CM000673.2:g.5226640_5226641delinsGC | GRCh38 |
NC_000011.9:g.5247870_5247871delinsGC , CM000673.1:g.5247870_5247871delinsGC | GRCh37 |
NC_000011.8:g.5204446_5204447delinsGC | NCBI36 |
NG_000007.3:g.70975_70976delinsGC | |
NG_059281.1:g.5431_5432delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.251_252delinsGC | ENSP00000494175.1:p.Gly84= | |
ENST00000335295.4:c.251_252delinsGC MANE Select | ENSP00000333994.3:p.Gly84= | |
ENST00000380315.2:c.251_252delinsGC | ENSP00000369671.2:p.Gly84= | |
ENST00000475226.1:n.183_184delinsGC | ||
ENST00000485743.1:n.302_303delinsGC | ||
ENST00000633227.1:c.*67_*68delinsGC | ENSP00000488004.1:n.*67_*68delinsGC | |
NM_000518.4:c.251_252delinsGC | NP_000509.1:p.Gly84= | |
NM_000518.5:c.251_252delinsGC MANE Select | NP_000509.1:p.Gly84= |