Canonical Allele Identifier: CA346725411
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs751264236
MyVariant Identifiers: chr2:g.47612350G>C (hg19) chr2:g.47385211G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47385211G>C , CM000664.2:g.47385211G>C GRCh38
NC_000002.11:g.47612350G>C , CM000664.1:g.47612350G>C GRCh37
NC_000002.10:g.47465854G>C NCBI36
NG_012352.2:g.45049G>C , LRG_215:g.45049G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263735.9:c.903+1G>C MANE Select ENSP00000263735.4:n.903+1G>C
ENST00000263735.8:c.903+1G>C ENSP00000263735.4:n.903+1G>C
ENST00000405271.5:c.987+1G>C ENSP00000385476.1:n.987+1G>C
ENST00000456133.5:c.987+1G>C ENSP00000410675.1:n.987+1G>C
NM_002354.2:c.903+1G>C , LRG_215t1:c.903+1G>C NP_002345.2:n.903+1G>C
NM_002354.3:c.903+1G>C MANE Select NP_002345.2:n.903+1G>C
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