Canonical Allele Identifier: CA2693426414

Gene: CYBB

Linked Data

• gnomAD v4: X-37795930-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795930G>C , CM000685.2:g.37795930G>C	GRCh38
NC_000023.10:g.37655183G>C , CM000685.1:g.37655183G>C	GRCh37
NC_000023.9:g.37540123G>C	NCBI36
NG_009065.1:g.20910G>C , LRG_53:g.20910G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-21G>C	ENSP00000512461.1:n.338-21G>C
ENST00000696171.1:c.388-21G>C	ENSP00000512462.1:n.388-21G>C
ENST00000696172.1:c.338-3025G>C	ENSP00000512463.1:n.338-3025G>C
ENST00000378588.5:c.484-21G>C MANE Select	ENSP00000367851.4:n.484-21G>C
ENST00000378588.4:c.484-21G>C	ENSP00000367851.4:n.484-21G>C
ENST00000465127.1:c.171+369930G>C	ENSP00000417050.1:n.171+369930G>C
NM_000397.3:c.484-21G>C , LRG_53t1:c.484-21G>C	NP_000388.2:n.484-21G>C
XM_011543890.1:c.178-21G>C	XP_011542192.1:n.178-21G>C
NM_000397.4:c.484-21G>C MANE Select	NP_000388.2:n.484-21G>C