Canonical Allele Identifier: CA1761188618
Gene: DEFB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877830T= , CM000670.2:g.6877830T= GRCh38
NC_000008.10:g.6735352T= , CM000670.1:g.6735352T= GRCh37
NC_000008.9:g.6722762T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297439.4:c.28A= MANE Select ENSP00000297439.3:p.Thr10=
ENST00000297439.3:c.28A= ENSP00000297439.3:p.Thr10=
NM_005218.3:c.28A= NP_005209.1:p.Thr10=
NM_005218.4:c.28A= MANE Select NP_005209.1:p.Thr10=
Search 100 bp 5'
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