Canonical Allele Identifier: CA744809710
Gene: EPPIN-WFDC6 HGNC NCBI
EPPIN HGNC NCBI

Linked Data

dbSNP Id: rs1308078783
gnomAD v3: 20-45547430-A-G
gnomAD v4: 20-45547430-A-G
MyVariant Identifiers: chr20:g.44176069A>G (hg19) chr20:g.45547430A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45547430A>G , CM000682.2:g.45547430A>G GRCh38
NC_000020.10:g.44176069A>G , CM000682.1:g.44176069A>G GRCh37
NC_000020.9:g.43609483A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651288.1:c.-73T>C (EPPIN-WFDC6) ENSP00000498632.1:n.-73T>C
ENST00000409554.1:c.-73T>C (EPPIN) ENSP00000387153.1:n.-73T>C
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