Canonical Allele Identifier: CA1761188622
Gene: DEFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877838A= , CM000670.2:g.6877838A= GRCh38
NC_000008.10:g.6735360A= , CM000670.1:g.6735360A= GRCh37
NC_000008.9:g.6722770A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.20T= MANE Select ENSP00000297439.3:p.Leu7=
ENST00000297439.3:c.20T= ENSP00000297439.3:p.Leu7=
NM_005218.3:c.20T= NP_005209.1:p.Leu7=
NM_005218.4:c.20T= MANE Select NP_005209.1:p.Leu7=