Canonical Allele Identifier: CA1761188508
Gene: DEFB1 HGNC NCBI

Linked Data

dbSNP Id: rs1806582801

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6877685C>G , CM000670.2:g.6877685C>G GRCh38
NC_000008.10:g.6735207C>G , CM000670.1:g.6735207C>G GRCh37
NC_000008.9:g.6722617C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297439.4:c.61+112G>C MANE Select ENSP00000297439.3:n.61+112G>C
ENST00000297439.3:c.61+112G>C ENSP00000297439.3:n.61+112G>C
NM_005218.3:c.61+112G>C NP_005209.1:n.61+112G>C
NM_005218.4:c.61+112G>C MANE Select NP_005209.1:n.61+112G>C