Canonical Allele Identifier: CA4612887
Gene: DEFB1 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.15C>G MANE Select ENSP00000297439.3:p.Tyr5Ter
ENST00000297439.3:c.15C>G ENSP00000297439.3:p.Tyr5Ter
NM_005218.3:c.15C>G NP_005209.1:p.Tyr5Ter
NM_005218.4:c.15C>G MANE Select NP_005209.1:p.Tyr5Ter