Canonical Allele Identifier: CA4612886
Gene: DEFB1 HGNC NCBI

Linked Data

dbSNP Id: rs759177517
gnomAD v2: 8-6735365-G-A
gnomAD v3: 8-6877843-G-A
gnomAD v4: 8-6877843-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877843G>A , CM000670.2:g.6877843G>A GRCh38
NC_000008.10:g.6735365G>A , CM000670.1:g.6735365G>A GRCh37
NC_000008.9:g.6722775G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.15C>T MANE Select ENSP00000297439.3:p.Tyr5=
ENST00000297439.3:c.15C>T ENSP00000297439.3:p.Tyr5=
NM_005218.3:c.15C>T NP_005209.1:p.Tyr5=
NM_005218.4:c.15C>T MANE Select NP_005209.1:p.Tyr5=