Canonical Allele Identifier: CA1761188596
Gene: DEFB1 HGNC NCBI

Linked Data

dbSNP Id: rs1585002855
gnomAD v4: 8-6877788-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877788A>G , CM000670.2:g.6877788A>G GRCh38
NC_000008.10:g.6735310A>G , CM000670.1:g.6735310A>G GRCh37
NC_000008.9:g.6722720A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.61+9T>C MANE Select ENSP00000297439.3:n.61+9T>C
ENST00000297439.3:c.61+9T>C ENSP00000297439.3:n.61+9T>C
NM_005218.3:c.61+9T>C NP_005209.1:n.61+9T>C
NM_005218.4:c.61+9T>C MANE Select NP_005209.1:n.61+9T>C