Canonical Allele Identifier: CA397065974
Community Standard Title: NM_000101.4(CYBA):c.84C>G (p.Ala28=)
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88648089G>C , CM000678.2:g.88648089G>C GRCh38
NC_000016.9:g.88714497G>C , CM000678.1:g.88714497G>C GRCh37
NC_000016.8:g.87241998G>C NCBI36
NG_007291.1:g.7961C>G , LRG_52:g.7961C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000101.4:c.84C>G MANE Select NP_000092.2:p.Ala28=
ENST00000261623.8:c.84C>G MANE Select ENSP00000261623.3:p.Ala28=
NM_000101.3:c.84C>G NP_000092.2:p.Ala28=
ENST00000261623.7:c.84C>G ENSP00000261623.3:p.Ala28=
ENST00000561972.1:n.125C>G
ENST00000562209.1:n.102C>G
ENST00000563526.5:n.59C>G
ENST00000565588.6:c.84C>G ENSP00000455537.2:p.Ala28=
ENST00000566229.1:c.73C>G ENSP00000457060.1:p.His25Asp
ENST00000566534.5:n.106C>G
ENST00000567174.5:c.84C>G ENSP00000454951.1:p.Ala28=
ENST00000568278.1:c.84C>G ENSP00000455506.1:p.Ala28=
ENST00000569359.5:c.84C>G ENSP00000456079.1:p.Ala28=
ENST00000696156.1:c.84C>G ENSP00000512446.1:p.Ala28=
ENST00000696157.1:c.84C>G ENSP00000512447.1:p.Ala28=
ENST00000696158.1:c.84C>G ENSP00000512448.1:p.Ala28=
ENST00000696159.1:c.84C>G ENSP00000512449.1:p.Ala28=
ENST00000696160.1:c.84C>G ENSP00000512450.1:p.Ala28=
ENST00000696161.1:c.84C>G ENSP00000512451.1:p.Ala28=
ENST00000696162.1:c.84C>G ENSP00000512452.1:p.Ala28=
ENST00000696163.1:c.84C>G ENSP00000512453.1:p.Ala28=
XM_011522905.1:c.84C>G XP_011521207.1:p.Ala28=
XM_011522905.3:c.84C>G XP_011521207.1:p.Ala28=