Canonical Allele Identifier: CA411799695

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43024276C>A (hg19) ; chr22:g.42628270C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628270C>A , CM000684.2:g.42628270C>A	GRCh38
NC_000022.10:g.43024276C>A , CM000684.1:g.43024276C>A	GRCh37
NC_000022.9:g.41354220C>A	NCBI36
NG_012194.1:g.26130G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.345G>T	ENSP00000354468.5:p.Lys115Asn
ENST00000402438.6:c.276G>T	ENSP00000385679.1:p.Lys92Asn
ENST00000407332.6:c.363G>T	ENSP00000384457.2:p.Lys121Asn
ENST00000407623.8:c.276G>T	ENSP00000384834.3:p.Lys92Asn
ENST00000438270.2:c.276G>T	ENSP00000403439.2:p.Lys92Asn
ENST00000684963.1:n.1622G>T
ENST00000686129.1:c.276G>T	ENSP00000508623.1:p.Lys92Asn
ENST00000686523.1:c.*294G>T	ENSP00000508940.1:n.*294G>T
ENST00000687183.1:n.406G>T
ENST00000687198.1:c.276G>T	ENSP00000508492.1:p.Lys92Asn
ENST00000688117.1:c.444G>T	ENSP00000509015.1:p.Lys148Asn
ENST00000688244.1:c.333+2612G>T	ENSP00000510355.1:n.333+2612G>T
ENST00000689001.1:n.752G>T
ENST00000689195.1:c.345G>T	ENSP00000509895.1:p.Lys115Asn
ENST00000689239.1:n.512G>T
ENST00000689795.1:n.507G>T
ENST00000690835.1:c.345G>T	ENSP00000509038.1:p.Lys115Asn
ENST00000690993.1:n.422G>T
ENST00000691295.1:c.334-582G>T	ENSP00000508706.1:n.334-582G>T
ENST00000691918.1:c.324G>T	ENSP00000509525.1:p.Lys108Asn
ENST00000692152.1:c.276G>T	ENSP00000509317.1:p.Lys92Asn
ENST00000692344.1:n.369G>T
ENST00000693157.1:c.265G>T	ENSP00000510610.1:n.265G>T
ENST00000693363.1:c.345G>T	ENSP00000510411.1:p.Lys115Asn
ENST00000693367.1:c.345G>T	ENSP00000508815.1:p.Lys115Asn
ENST00000693639.1:c.338G>T	ENSP00000510223.1:p.Arg113Met
ENST00000693646.1:c.251G>T	ENSP00000508449.1:p.Arg84Met
ENST00000352397.10:c.345G>T MANE Select	ENSP00000338461.6:p.Lys115Asn
ENST00000352397.9:c.345G>T	ENSP00000338461.6:p.Lys115Asn
ENST00000361740.8:c.444G>T	ENSP00000354468.4:p.Lys148Asn
ENST00000402438.5:c.276G>T	ENSP00000385679.1:p.Lys92Asn
ENST00000407332.5:c.276G>T	ENSP00000384457.1:p.Lys92Asn
ENST00000407623.7:c.276G>T	ENSP00000384834.3:p.Lys92Asn
ENST00000438270.1:c.276G>T	ENSP00000403439.1:p.Lys92Asn
ENST00000470741.1:n.2479G>T
NM_000398.6:c.345G>T	NP_000389.1:p.Lys115Asn
NM_001129819.2:c.276G>T	NP_001123291.1:p.Lys92Asn
NM_001171660.1:c.444G>T	NP_001165131.1:p.Lys148Asn
NM_001171661.1:c.276G>T	NP_001165132.1:p.Lys92Asn
NM_007326.4:c.276G>T	NP_015565.1:p.Lys92Asn
NM_000398.7:c.345G>T MANE Select	NP_000389.1:p.Lys115Asn
NM_001171660.2:c.444G>T	NP_001165131.1:p.Lys148Asn