Canonical Allele Identifier: CA4612881
Gene: DEFB1 HGNC NCBI

Linked Data

dbSNP Id: rs549676840
gnomAD v2: 8-6735349-G-C
gnomAD v3: 8-6877827-G-C
gnomAD v4: 8-6877827-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877827G>C , CM000670.2:g.6877827G>C GRCh38
NC_000008.10:g.6735349G>C , CM000670.1:g.6735349G>C GRCh37
NC_000008.9:g.6722759G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.31C>G MANE Select ENSP00000297439.3:p.Leu11Val
ENST00000297439.3:c.31C>G ENSP00000297439.3:p.Leu11Val
NM_005218.3:c.31C>G NP_005209.1:p.Leu11Val
NM_005218.4:c.31C>G MANE Select NP_005209.1:p.Leu11Val