Canonical Allele Identifier: CA743720002
Gene: BPIFB1 HGNC NCBI

Linked Data

dbSNP Id: rs1324587245
MyVariant Identifiers: chr20:g.31863013A>C (hg19) chr20:g.33275207A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33275207A>C , CM000682.2:g.33275207A>C GRCh38
NC_000020.10:g.31863013A>C , CM000682.1:g.31863013A>C GRCh37
NC_000020.9:g.31326674A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423645.5:c.-42+1553A>C ENSP00000390471.1:n.-42+1553A>C
XM_024452018.1:c.-295+1553A>C XP_024307786.1:n.-295+1553A>C
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