Canonical Allele Identifier: CA1761188562
Gene: DEFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877748T= , CM000670.2:g.6877748T= GRCh38
NC_000008.10:g.6735270T= , CM000670.1:g.6735270T= GRCh37
NC_000008.9:g.6722680T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297439.4:c.61+49A= MANE Select ENSP00000297439.3:n.61+49A=
ENST00000297439.3:c.61+49A= ENSP00000297439.3:n.61+49A=
NM_005218.3:c.61+49A= NP_005209.1:n.61+49A=
NM_005218.4:c.61+49A= MANE Select NP_005209.1:n.61+49A=