Canonical Allele Identifier: CA411799339

Gene: CYB5R3

Linked Data

• gnomAD v4: 22-42628215-T-C
• MyVariant Identifiers: chr22:g.43024221T>C (hg19) ; chr22:g.42628215T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628215T>C , CM000684.2:g.42628215T>C	GRCh38
NC_000022.10:g.43024221T>C , CM000684.1:g.43024221T>C	GRCh37
NC_000022.9:g.41354165T>C	NCBI36
NG_012194.1:g.26185A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.400A>G	ENSP00000354468.5:p.Met134Val
ENST00000402438.6:c.331A>G	ENSP00000385679.1:p.Met111Val
ENST00000407332.6:c.418A>G	ENSP00000384457.2:p.Met140Val
ENST00000407623.8:c.331A>G	ENSP00000384834.3:p.Met111Val
ENST00000438270.2:c.331A>G	ENSP00000403439.2:p.Met111Val
ENST00000684963.1:n.1677A>G
ENST00000686129.1:c.331A>G	ENSP00000508623.1:p.Met111Val
ENST00000686523.1:c.*349A>G	ENSP00000508940.1:n.*349A>G
ENST00000687183.1:n.461A>G
ENST00000687198.1:c.331A>G	ENSP00000508492.1:p.Met111Val
ENST00000688117.1:c.499A>G	ENSP00000509015.1:p.Met167Val
ENST00000688244.1:c.333+2667A>G	ENSP00000510355.1:n.333+2667A>G
ENST00000689001.1:n.807A>G
ENST00000689195.1:c.400A>G	ENSP00000509895.1:p.Met134Val
ENST00000689239.1:n.567A>G
ENST00000689795.1:n.562A>G
ENST00000690835.1:c.400A>G	ENSP00000509038.1:p.Met134Val
ENST00000690993.1:n.477A>G
ENST00000691295.1:c.334-527A>G	ENSP00000508706.1:n.334-527A>G
ENST00000691918.1:c.379A>G	ENSP00000509525.1:p.Met127Val
ENST00000692152.1:c.331A>G	ENSP00000509317.1:p.Met111Val
ENST00000692344.1:n.424A>G
ENST00000693157.1:c.320A>G	ENSP00000510610.1:n.320A>G
ENST00000693363.1:c.400A>G	ENSP00000510411.1:p.Met134Val
ENST00000693367.1:c.400A>G	ENSP00000508815.1:p.Met134Val
ENST00000693639.1:c.393A>G	ENSP00000510223.1:p.Ala131=
ENST00000693646.1:c.306A>G	ENSP00000508449.1:p.Ala102=
ENST00000352397.10:c.400A>G MANE Select	ENSP00000338461.6:p.Met134Val
ENST00000352397.9:c.400A>G	ENSP00000338461.6:p.Met134Val
ENST00000361740.8:c.499A>G	ENSP00000354468.4:p.Met167Val
ENST00000402438.5:c.331A>G	ENSP00000385679.1:p.Met111Val
ENST00000407332.5:c.331A>G	ENSP00000384457.1:p.Met111Val
ENST00000407623.7:c.331A>G	ENSP00000384834.3:p.Met111Val
ENST00000438270.1:c.331A>G	ENSP00000403439.1:p.Met111Val
ENST00000470741.1:n.2534A>G
NM_000398.6:c.400A>G	NP_000389.1:p.Met134Val
NM_001129819.2:c.331A>G	NP_001123291.1:p.Met111Val
NM_001171660.1:c.499A>G	NP_001165131.1:p.Met167Val
NM_001171661.1:c.331A>G	NP_001165132.1:p.Met111Val
NM_007326.4:c.331A>G	NP_015565.1:p.Met111Val
NM_000398.7:c.400A>G MANE Select	NP_000389.1:p.Met134Val
NM_001171660.2:c.499A>G	NP_001165131.1:p.Met167Val