Canonical Allele Identifier: CA411800622
Gene: CYB5R3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42630964C>G , CM000684.2:g.42630964C>G GRCh38
NC_000022.10:g.43026970C>G , CM000684.1:g.43026970C>G GRCh37
NC_000022.9:g.41356914C>G NCBI36
NG_012194.1:g.23436G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.251G>C ENSP00000354468.5:p.Arg84Pro
ENST00000402438.6:c.182G>C ENSP00000385679.1:p.Arg61Pro
ENST00000407332.6:c.269G>C ENSP00000384457.2:p.Arg90Pro
ENST00000407623.8:c.182G>C ENSP00000384834.3:p.Arg61Pro
ENST00000438270.2:c.182G>C ENSP00000403439.2:p.Arg61Pro
ENST00000466276.2:n.318G>C
ENST00000686129.1:c.182G>C ENSP00000508623.1:p.Arg61Pro
ENST00000686523.1:c.*200G>C ENSP00000508940.1:n.*200G>C
ENST00000687183.1:n.312G>C
ENST00000687198.1:c.182G>C ENSP00000508492.1:p.Arg61Pro
ENST00000688117.1:c.350G>C ENSP00000509015.1:p.Arg117Pro
ENST00000688244.1:c.251G>C ENSP00000510355.1:p.Arg84Pro
ENST00000689001.1:n.658G>C
ENST00000689195.1:c.251G>C ENSP00000509895.1:p.Arg84Pro
ENST00000689239.1:n.418G>C
ENST00000689795.1:n.413G>C
ENST00000690835.1:c.251G>C ENSP00000509038.1:p.Arg84Pro
ENST00000690993.1:n.328G>C
ENST00000691295.1:c.251G>C ENSP00000508706.1:p.Arg84Pro
ENST00000691918.1:c.230G>C ENSP00000509525.1:p.Arg77Pro
ENST00000692152.1:c.182G>C ENSP00000509317.1:p.Arg61Pro
ENST00000692344.1:n.275G>C
ENST00000693157.1:c.171G>C ENSP00000510610.1:p.Ser57=
ENST00000693363.1:c.251G>C ENSP00000510411.1:p.Arg84Pro
ENST00000693367.1:c.251G>C ENSP00000508815.1:p.Arg84Pro
ENST00000693639.1:c.244G>C ENSP00000510223.1:p.Glu82Gln
ENST00000693646.1:c.157G>C ENSP00000508449.1:p.Glu53Gln
ENST00000693716.1:n.479G>C
ENST00000352397.10:c.251G>C MANE Select ENSP00000338461.6:p.Arg84Pro
ENST00000352397.9:c.251G>C ENSP00000338461.6:p.Arg84Pro
ENST00000361740.8:c.350G>C ENSP00000354468.4:p.Arg117Pro
ENST00000402438.5:c.182G>C ENSP00000385679.1:p.Arg61Pro
ENST00000407332.5:c.182G>C ENSP00000384457.1:p.Arg61Pro
ENST00000407623.7:c.182G>C ENSP00000384834.3:p.Arg61Pro
ENST00000438270.1:c.182G>C ENSP00000403439.1:p.Arg61Pro
ENST00000470741.1:n.2385G>C
NM_000398.6:c.251G>C NP_000389.1:p.Arg84Pro
NM_001129819.2:c.182G>C NP_001123291.1:p.Arg61Pro
NM_001171660.1:c.350G>C NP_001165131.1:p.Arg117Pro
NM_001171661.1:c.182G>C NP_001165132.1:p.Arg61Pro
NM_007326.4:c.182G>C NP_015565.1:p.Arg61Pro
NM_000398.7:c.251G>C MANE Select NP_000389.1:p.Arg84Pro
NM_001171660.2:c.350G>C NP_001165131.1:p.Arg117Pro