Canonical Allele Identifier: CA46641954
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs987245397
MyVariant Identifiers: chr2:g.47377124G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377124G>C , CM000664.2:g.47377124G>C GRCh38
NC_000002.11:g.47604263G>C , CM000664.1:g.47604263G>C GRCh37
NC_000002.10:g.47457767G>C NCBI36
NG_012352.2:g.36962G>C , LRG_215:g.36962G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+47G>C MANE Select ENSP00000263735.4:n.555+47G>C
ENST00000263735.8:c.555+47G>C ENSP00000263735.4:n.555+47G>C
ENST00000405271.5:c.639+47G>C ENSP00000385476.1:n.639+47G>C
ENST00000456133.5:c.639+47G>C ENSP00000410675.1:n.639+47G>C
ENST00000490733.1:n.404+47G>C
NM_002354.2:c.555+47G>C , LRG_215t1:c.555+47G>C NP_002345.2:n.555+47G>C
NM_002354.3:c.555+47G>C MANE Select NP_002345.2:n.555+47G>C
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