Canonical Allele Identifier: CA2695233137

Gene: CYBB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37803886_37803890delinsAACCG , CM000685.2:g.37803886_37803890delinsAACCG	GRCh38
NC_000023.10:g.37663139_37663143delinsAACCG , CM000685.1:g.37663139_37663143delinsAACCG	GRCh37
NC_000023.9:g.37548083_37548087delinsAACCG	NCBI36
NG_009065.1:g.28870_28874delinsAACCG , LRG_53:g.28870_28874delinsAACCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000696170.1:c.*416_*420delinsAACCG	ENSP00000512461.1:n.*416_*420delinsAACCG
ENST00000696171.1:c.811_815delinsAACCG	ENSP00000512462.1:p.His271_Pro272delinsAs...
ENST00000378588.5:c.907_911delinsAACCG MANE Select	ENSP00000367851.4:p.His303_Pro304delinsAs...
ENST00000378588.4:c.907_911delinsAACCG	ENSP00000367851.4:p.His303_Pro304delinsAs...
ENST00000465127.1:c.171+377886_171+377890delinsAACCG	ENSP00000417050.1:n.171+377886_171+377890...
ENST00000492288.1:n.332_336delinsAACCG
NM_000397.3:c.907_911delinsAACCG , LRG_53t1:c.907_911delinsAACCG	NP_000388.2:p.His303_Pro304delinsAsnArg
XM_011543890.1:c.601_605delinsAACCG	XP_011542192.1:p.His201_Pro202delinsAsnAr...
NM_000397.4:c.907_911delinsAACCG MANE Select	NP_000388.2:p.His303_Pro304delinsAsnArg