Canonical Allele Identifier: CA459186468
Gene: DEFB1 HGNC NCBI

Linked Data

dbSNP Id: rs1806591255
MyVariant Identifiers: chr8:g.6735361G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877839G>A , CM000670.2:g.6877839G>A GRCh38
NC_000008.10:g.6735361G>A , CM000670.1:g.6735361G>A GRCh37
NC_000008.9:g.6722771G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.19C>T MANE Select ENSP00000297439.3:p.Leu7=
ENST00000297439.3:c.19C>T ENSP00000297439.3:p.Leu7=
NM_005218.3:c.19C>T NP_005209.1:p.Leu7=
NM_005218.4:c.19C>T MANE Select NP_005209.1:p.Leu7=