Canonical Allele Identifier: CA2543006705

Gene: CYBB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795898_37795899insCGTG , CM000685.2:g.37795898_37795899insCGTG	GRCh38
NC_000023.10:g.37655151_37655152insCGTG , CM000685.1:g.37655151_37655152insCGTG	GRCh37
NC_000023.9:g.37540091_37540092insCGTG	NCBI36
NG_009065.1:g.20878_20879insCGTG , LRG_53:g.20878_20879insCGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-53_338-52insCGTG	ENSP00000512461.1:n.338-53_338-52insCGTG
ENST00000696171.1:c.388-53_388-52insCGTG	ENSP00000512462.1:n.388-53_388-52insCGTG
ENST00000696172.1:c.338-3057_338-3056insCGTG	ENSP00000512463.1:n.338-3057_338-3056insCGTG
ENST00000378588.5:c.484-53_484-52insCGTG MANE Select	ENSP00000367851.4:n.484-53_484-52insCGTG
ENST00000378588.4:c.484-53_484-52insCGTG	ENSP00000367851.4:n.484-53_484-52insCGTG
ENST00000465127.1:c.171+369898_171+369899insCGTG	ENSP00000417050.1:n.171+369898_171+369899insCGTG
NM_000397.3:c.484-53_484-52insCGTG , LRG_53t1:c.484-53_484-52insCGTG	NP_000388.2:n.484-53_484-52insCGTG
XM_011543890.1:c.178-53_178-52insCGTG	XP_011542192.1:n.178-53_178-52insCGTG
NM_000397.4:c.484-53_484-52insCGTG MANE Select	NP_000388.2:n.484-53_484-52insCGTG