Canonical Allele Identifier: CA412977458

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37663328T>C (hg19) ; chrX:g.37804075T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37804075T>C , CM000685.2:g.37804075T>C	GRCh38
NC_000023.10:g.37663328T>C , CM000685.1:g.37663328T>C	GRCh37
NC_000023.9:g.37548272T>C	NCBI36
NG_009065.1:g.29059T>C , LRG_53:g.29059T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*605T>C	ENSP00000512461.1:n.*605T>C
ENST00000696171.1:c.1000T>C	ENSP00000512462.1:p.Phe334Leu
ENST00000378588.5:c.1096T>C MANE Select	ENSP00000367851.4:p.Phe366Leu
ENST00000378588.4:c.1096T>C	ENSP00000367851.4:p.Phe366Leu
ENST00000465127.1:c.171+378075T>C	ENSP00000417050.1:n.171+378075T>C
ENST00000492288.1:n.521T>C
NM_000397.3:c.1096T>C , LRG_53t1:c.1096T>C	NP_000388.2:p.Phe366Leu
XM_011543890.1:c.790T>C	XP_011542192.1:p.Phe264Leu
NM_000397.4:c.1096T>C MANE Select	NP_000388.2:p.Phe366Leu