Canonical Allele Identifier: CA4612882
Gene: DEFB1 HGNC NCBI

Linked Data

dbSNP Id: rs772872367
gnomAD v2: 8-6735351-G-C
gnomAD v4: 8-6877829-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877829G>C , CM000670.2:g.6877829G>C GRCh38
NC_000008.10:g.6735351G>C , CM000670.1:g.6735351G>C GRCh37
NC_000008.9:g.6722761G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.29C>G MANE Select ENSP00000297439.3:p.Thr10Ser
ENST00000297439.3:c.29C>G ENSP00000297439.3:p.Thr10Ser
NM_005218.3:c.29C>G NP_005209.1:p.Thr10Ser
NM_005218.4:c.29C>G MANE Select NP_005209.1:p.Thr10Ser