Canonical Allele Identifier: CA397064911

Gene: CYBA

Linked Data

• gnomAD v4: 16-88647106-C-A
• MyVariant Identifiers: chr16:g.88713514C>A (hg19) ; chr16:g.88647106C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88647106C>A , CM000678.2:g.88647106C>A	GRCh38
NC_000016.9:g.88713514C>A , CM000678.1:g.88713514C>A	GRCh37
NC_000016.8:g.87241015C>A	NCBI36
NG_007291.1:g.8944G>T , LRG_52:g.8944G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565588.6:c.198G>T	ENSP00000455537.2:p.Glu66Asp
ENST00000696156.1:c.198G>T	ENSP00000512446.1:p.Glu66Asp
ENST00000696157.1:c.198G>T	ENSP00000512447.1:p.Glu66Asp
ENST00000696158.1:c.198G>T	ENSP00000512448.1:p.Glu66Asp
ENST00000696159.1:c.198G>T	ENSP00000512449.1:p.Glu66Asp
ENST00000696160.1:c.198G>T	ENSP00000512450.1:p.Glu66Asp
ENST00000696161.1:c.198G>T	ENSP00000512451.1:p.Glu66Asp
ENST00000696162.1:c.198G>T	ENSP00000512452.1:p.Glu66Asp
ENST00000696163.1:c.198G>T	ENSP00000512453.1:p.Glu66Asp
ENST00000261623.8:c.198G>T MANE Select	ENSP00000261623.3:p.Glu66Asp
ENST00000261623.7:c.198G>T	ENSP00000261623.3:p.Glu66Asp
ENST00000562209.1:n.216G>T
ENST00000563526.5:n.173G>T
ENST00000566229.1:c.187G>T	ENSP00000457060.1:p.Ala63Ser
ENST00000566534.5:n.220G>T
ENST00000567174.5:c.198G>T	ENSP00000454951.1:p.Glu66Asp
ENST00000568278.1:c.198G>T	ENSP00000455506.1:p.Glu66Asp
ENST00000569359.5:c.198G>T	ENSP00000456079.1:p.Glu66Asp
NM_000101.3:c.198G>T	NP_000092.2:p.Glu66Asp
XM_011522905.1:c.198G>T	XP_011521207.1:p.Glu66Asp
XM_011522905.3:c.198G>T	XP_011521207.1:p.Glu66Asp
NM_000101.4:c.198G>T MANE Select	NP_000092.2:p.Glu66Asp