Canonical Allele Identifier: CA2693426398

Gene: CYBB

Linked Data

• gnomAD v4: X-37795919-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795919T>C , CM000685.2:g.37795919T>C	GRCh38
NC_000023.10:g.37655172T>C , CM000685.1:g.37655172T>C	GRCh37
NC_000023.9:g.37540112T>C	NCBI36
NG_009065.1:g.20899T>C , LRG_53:g.20899T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-32T>C	ENSP00000512461.1:n.338-32T>C
ENST00000696171.1:c.388-32T>C	ENSP00000512462.1:n.388-32T>C
ENST00000696172.1:c.338-3036T>C	ENSP00000512463.1:n.338-3036T>C
ENST00000378588.5:c.484-32T>C MANE Select	ENSP00000367851.4:n.484-32T>C
ENST00000378588.4:c.484-32T>C	ENSP00000367851.4:n.484-32T>C
ENST00000465127.1:c.171+369919T>C	ENSP00000417050.1:n.171+369919T>C
NM_000397.3:c.484-32T>C , LRG_53t1:c.484-32T>C	NP_000388.2:n.484-32T>C
XM_011543890.1:c.178-32T>C	XP_011542192.1:n.178-32T>C
NM_000397.4:c.484-32T>C MANE Select	NP_000388.2:n.484-32T>C