Canonical Allele Identifier: CA743719967
Gene: BPIFB1 HGNC NCBI

Linked Data

dbSNP Id: rs1346371483
MyVariant Identifiers: chr20:g.31862904C>T (hg19) chr20:g.33275098C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33275098C>T , CM000682.2:g.33275098C>T GRCh38
NC_000020.10:g.31862904C>T , CM000682.1:g.31862904C>T GRCh37
NC_000020.9:g.31326565C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000423645.5:c.-42+1444C>T ENSP00000390471.1:n.-42+1444C>T
XM_024452018.1:c.-295+1444C>T XP_024307786.1:n.-295+1444C>T
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