Canonical Allele Identifier: CA412972769

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37642783A>C (hg19) ; chrX:g.37783530A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783530A>C , CM000685.2:g.37783530A>C	GRCh38
NC_000023.10:g.37642783A>C , CM000685.1:g.37642783A>C	GRCh37
NC_000023.9:g.37527727A>C	NCBI36
NG_009065.1:g.8514A>C , LRG_53:g.8514A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.182A>C	ENSP00000512461.1:p.Asn61Thr
ENST00000696171.1:c.86A>C	ENSP00000512462.1:p.Asn29Thr
ENST00000696172.1:c.182A>C	ENSP00000512463.1:p.Asn61Thr
ENST00000696173.1:n.190A>C
ENST00000378588.5:c.182A>C MANE Select	ENSP00000367851.4:p.Asn61Thr
ENST00000378588.4:c.182A>C	ENSP00000367851.4:p.Asn61Thr
ENST00000465127.1:c.171+357530A>C	ENSP00000417050.1:n.171+357530A>C
NM_000397.3:c.182A>C , LRG_53t1:c.182A>C	NP_000388.2:p.Asn61Thr
XM_011543890.1:c.-249A>C	XP_011542192.1:n.-249A>C
NM_000397.4:c.182A>C MANE Select	NP_000388.2:p.Asn61Thr