Canonical Allele Identifier: CA2695232431

Gene: CYBB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783478delinsACCTCTTCTAG , CM000685.2:g.37783478delinsACCTCTTCTAG	GRCh38
NC_000023.10:g.37642731delinsACCTCTTCTAG , CM000685.1:g.37642731delinsACCTCTTCTAG	GRCh37
NC_000023.9:g.37527675delinsACCTCTTCTAG	NCBI36
NG_009065.1:g.8462delinsACCTCTTCTAG , LRG_53:g.8462delinsACCTCTTCTAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000696170.1:c.142-12delinsACCTCTTCTAG	ENSP00000512461.1:n.142-12delinsACCTCTTCTAG
ENST00000696171.1:c.46-12delinsACCTCTTCTAG	ENSP00000512462.1:n.46-12delinsACCTCTTCTAG
ENST00000696172.1:c.142-12delinsACCTCTTCTAG	ENSP00000512463.1:n.142-12delinsACCTCTTCTAG
ENST00000696173.1:n.150-12delinsACCTCTTCTAG
ENST00000378588.5:c.142-12delinsACCTCTTCTAG MANE Select	ENSP00000367851.4:n.142-12delinsACCTCTTCTAG
ENST00000378588.4:c.142-12delinsACCTCTTCTAG	ENSP00000367851.4:n.142-12delinsACCTCTTCTAG
ENST00000465127.1:c.171+357478delinsACCTCTTCTAG	ENSP00000417050.1:n.171+357478delinsACCTCTTCTAG
NM_000397.3:c.142-12delinsACCTCTTCTAG , LRG_53t1:c.142-12delinsACCTCTTCTAG	NP_000388.2:n.142-12delinsACCTCTTCTAG
XM_011543890.1:c.-289-12delinsACCTCTTCTAG	XP_011542192.1:n.-289-12delinsACCTCTTCTAG
NM_000397.4:c.142-12delinsACCTCTTCTAG MANE Select	NP_000388.2:n.142-12delinsACCTCTTCTAG