Canonical Allele Identifier: CA171486222
Gene: DEFB1 HGNC NCBI

Linked Data

dbSNP Id: rs755715533
gnomAD v2: 8-6735352-T-G
gnomAD v3: 8-6877830-T-G
gnomAD v4: 8-6877830-T-G

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.28A>C MANE Select ENSP00000297439.3:p.Thr10Pro
ENST00000297439.3:c.28A>C ENSP00000297439.3:p.Thr10Pro
NM_005218.3:c.28A>C NP_005209.1:p.Thr10Pro
NM_005218.4:c.28A>C MANE Select NP_005209.1:p.Thr10Pro