Canonical Allele Identifier: CA313244784
Gene: BPIFB1 HGNC NCBI

Linked Data

dbSNP Id: rs892263779
gnomAD v3: 20-33275199-G-A
gnomAD v4: 20-33275199-G-A
MyVariant Identifiers: chr20:g.31863005G>A (hg19) chr20:g.33275199G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33275199G>A , CM000682.2:g.33275199G>A GRCh38
NC_000020.10:g.31863005G>A , CM000682.1:g.31863005G>A GRCh37
NC_000020.9:g.31326666G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423645.5:c.-42+1545G>A ENSP00000390471.1:n.-42+1545G>A
XM_024452018.1:c.-295+1545G>A XP_024307786.1:n.-295+1545G>A
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