Canonical Allele Identifier: CA769407832
Gene: EPCAM-DT HGNC NCBI

Linked Data

dbSNP Id: rs1199291014
gnomAD v3: 2-47254334-C-T
gnomAD v4: 2-47254334-C-T
MyVariant Identifiers: chr2:g.47481473C>T (hg19) chr2:g.47254334C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47254334C>T , CM000664.2:g.47254334C>T GRCh38
NC_000002.11:g.47481473C>T , CM000664.1:g.47481473C>T GRCh37
NC_000002.10:g.47334977C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110207.1:n.175-33011G>A
NR_110208.1:n.404-54791G>A
XR_001739451.1:n.606-1449G>A
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