Canonical Allele Identifier: CA349282622
Gene: CYBRD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.171554764T>A , CM000664.2:g.171554764T>A GRCh38
NC_000002.11:g.172411274T>A , CM000664.1:g.172411274T>A GRCh37
NC_000002.10:g.172119520T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000321348.9:c.798T>A MANE Select ENSP00000319141.4:p.Ser266Arg
ENST00000321348.8:c.798T>A ENSP00000319141.4:p.Ser266Arg
ENST00000375252.3:c.*115T>A ENSP00000364401.3:n.*115T>A
ENST00000409484.5:c.624T>A ENSP00000386739.1:p.Ser208Arg
NM_001127383.1:c.*115T>A NP_001120855.1:n.*115T>A
NM_001256909.1:c.624T>A NP_001243838.1:p.Ser208Arg
NM_024843.3:c.798T>A NP_079119.3:p.Ser266Arg
NM_024843.4:c.798T>A MANE Select NP_079119.3:p.Ser266Arg
NM_001127383.2:c.*115T>A NP_001120855.1:n.*115T>A
NM_001256909.2:c.624T>A NP_001243838.1:p.Ser208Arg