Canonical Allele Identifier: CA1761188612
Gene: DEFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877823C= , CM000670.2:g.6877823C= GRCh38
NC_000008.10:g.6735345C= , CM000670.1:g.6735345C= GRCh37
NC_000008.9:g.6722755C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.35G= MANE Select ENSP00000297439.3:p.Cys12=
ENST00000297439.3:c.35G= ENSP00000297439.3:p.Cys12=
NM_005218.3:c.35G= NP_005209.1:p.Cys12=
NM_005218.4:c.35G= MANE Select NP_005209.1:p.Cys12=