Canonical Allele Identifier: CA4612878
Gene: DEFB1 HGNC NCBI

Linked Data

dbSNP Id: rs761637452
gnomAD v2: 8-6735344-G-A
gnomAD v4: 8-6877822-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877822G>A , CM000670.2:g.6877822G>A GRCh38
NC_000008.10:g.6735344G>A , CM000670.1:g.6735344G>A GRCh37
NC_000008.9:g.6722754G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.36C>T MANE Select ENSP00000297439.3:p.Cys12=
ENST00000297439.3:c.36C>T ENSP00000297439.3:p.Cys12=
NM_005218.3:c.36C>T NP_005209.1:p.Cys12=
NM_005218.4:c.36C>T MANE Select NP_005209.1:p.Cys12=