Canonical Allele Identifier: CA429777655
Gene: CYBRD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.172411277A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.171554767A>G , CM000664.2:g.171554767A>G GRCh38
NC_000002.11:g.172411277A>G , CM000664.1:g.172411277A>G GRCh37
NC_000002.10:g.172119523A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321348.9:c.801A>G MANE Select ENSP00000319141.4:p.Glu267=
ENST00000321348.8:c.801A>G ENSP00000319141.4:p.Glu267=
ENST00000375252.3:c.*118A>G ENSP00000364401.3:n.*118A>G
ENST00000409484.5:c.627A>G ENSP00000386739.1:p.Glu209=
NM_001127383.1:c.*118A>G NP_001120855.1:n.*118A>G
NM_001256909.1:c.627A>G NP_001243838.1:p.Glu209=
NM_024843.3:c.801A>G NP_079119.3:p.Glu267=
NM_024843.4:c.801A>G MANE Select NP_079119.3:p.Glu267=
NM_001127383.2:c.*118A>G NP_001120855.1:n.*118A>G
NM_001256909.2:c.627A>G NP_001243838.1:p.Glu209=
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