Canonical Allele Identifier: CA397064964
Gene: CYBA HGNC NCBI

Linked Data

dbSNP Id: rs775610308

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88647121C>G , CM000678.2:g.88647121C>G GRCh38
NC_000016.9:g.88713529C>G , CM000678.1:g.88713529C>G GRCh37
NC_000016.8:g.87241030C>G NCBI36
NG_007291.1:g.8929G>C , LRG_52:g.8929G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000565588.6:c.183G>C ENSP00000455537.2:p.Lys61Asn
ENST00000696156.1:c.183G>C ENSP00000512446.1:p.Lys61Asn
ENST00000696157.1:c.183G>C ENSP00000512447.1:p.Lys61Asn
ENST00000696158.1:c.183G>C ENSP00000512448.1:p.Lys61Asn
ENST00000696159.1:c.183G>C ENSP00000512449.1:p.Lys61Asn
ENST00000696160.1:c.183G>C ENSP00000512450.1:p.Lys61Asn
ENST00000696161.1:c.183G>C ENSP00000512451.1:p.Lys61Asn
ENST00000696162.1:c.183G>C ENSP00000512452.1:p.Lys61Asn
ENST00000696163.1:c.183G>C ENSP00000512453.1:p.Lys61Asn
ENST00000261623.8:c.183G>C MANE Select ENSP00000261623.3:p.Lys61Asn
ENST00000261623.7:c.183G>C ENSP00000261623.3:p.Lys61Asn
ENST00000562209.1:n.201G>C
ENST00000563526.5:n.158G>C
ENST00000566229.1:c.172G>C ENSP00000457060.1:p.Gly58Arg
ENST00000566534.5:n.205G>C
ENST00000567174.5:c.183G>C ENSP00000454951.1:p.Lys61Asn
ENST00000568278.1:c.183G>C ENSP00000455506.1:p.Lys61Asn
ENST00000569359.5:c.183G>C ENSP00000456079.1:p.Lys61Asn
NM_000101.3:c.183G>C NP_000092.2:p.Lys61Asn
XM_011522905.1:c.183G>C XP_011521207.1:p.Lys61Asn
XM_011522905.3:c.183G>C XP_011521207.1:p.Lys61Asn
NM_000101.4:c.183G>C MANE Select NP_000092.2:p.Lys61Asn