Canonical Allele Identifier: CA2693426410

Gene: CYBB

Linked Data

• gnomAD v4: X-37795928-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795929_37795930insTT , CM000685.2:g.37795929_37795930insTT	GRCh38
NC_000023.10:g.37655182_37655183insTT , CM000685.1:g.37655182_37655183insTT	GRCh37
NC_000023.9:g.37540122_37540123insTT	NCBI36
NG_009065.1:g.20909_20910insTT , LRG_53:g.20909_20910insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-22_338-21insTT	ENSP00000512461.1:n.338-22_338-21insTT
ENST00000696171.1:c.388-22_388-21insTT	ENSP00000512462.1:n.388-22_388-21insTT
ENST00000696172.1:c.338-3026_338-3025insTT	ENSP00000512463.1:n.338-3026_338-3025insTT
ENST00000378588.5:c.484-22_484-21insTT MANE Select	ENSP00000367851.4:n.484-22_484-21insTT
ENST00000378588.4:c.484-22_484-21insTT	ENSP00000367851.4:n.484-22_484-21insTT
ENST00000465127.1:c.171+369929_171+369930insTT	ENSP00000417050.1:n.171+369929_171+369930insTT
NM_000397.3:c.484-22_484-21insTT , LRG_53t1:c.484-22_484-21insTT	NP_000388.2:n.484-22_484-21insTT
XM_011543890.1:c.178-22_178-21insTT	XP_011542192.1:n.178-22_178-21insTT
NM_000397.4:c.484-22_484-21insTT MANE Select	NP_000388.2:n.484-22_484-21insTT