Canonical Allele Identifier: CA459186428
Gene: DEFB1 HGNC NCBI

Linked Data

gnomAD v4: 8-6877834-C-G
MyVariant Identifiers: chr8:g.6735356C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877834C>G , CM000670.2:g.6877834C>G GRCh38
NC_000008.10:g.6735356C>G , CM000670.1:g.6735356C>G GRCh37
NC_000008.9:g.6722766C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.24G>C MANE Select ENSP00000297439.3:p.Leu8=
ENST00000297439.3:c.24G>C ENSP00000297439.3:p.Leu8=
NM_005218.3:c.24G>C NP_005209.1:p.Leu8=
NM_005218.4:c.24G>C MANE Select NP_005209.1:p.Leu8=