Canonical Allele Identifier: CA769444142
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs1482876629
gnomAD v4: 2-47376982-T-G
MyVariant Identifiers: chr2:g.47604121T>G (hg19) chr2:g.47376982T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47376982T>G , CM000664.2:g.47376982T>G GRCh38
NC_000002.11:g.47604121T>G , CM000664.1:g.47604121T>G GRCh37
NC_000002.10:g.47457625T>G NCBI36
NG_012352.2:g.36820T>G , LRG_215:g.36820T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.492-32T>G MANE Select ENSP00000263735.4:n.492-32T>G
ENST00000263735.8:c.492-32T>G ENSP00000263735.4:n.492-32T>G
ENST00000405271.5:c.576-32T>G ENSP00000385476.1:n.576-32T>G
ENST00000456133.5:c.576-32T>G ENSP00000410675.1:n.576-32T>G
ENST00000490733.1:n.341-32T>G
NM_002354.2:c.492-32T>G , LRG_215t1:c.492-32T>G NP_002345.2:n.492-32T>G
NM_002354.3:c.492-32T>G MANE Select NP_002345.2:n.492-32T>G
Search 100 bp 5'
Search 100 bp 3'