Canonical Allele Identifier: CA346723968
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs2103753310
MyVariant Identifiers: chr2:g.47604166G>C (hg19) chr2:g.47377027G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377027G>C , CM000664.2:g.47377027G>C GRCh38
NC_000002.11:g.47604166G>C , CM000664.1:g.47604166G>C GRCh37
NC_000002.10:g.47457670G>C NCBI36
NG_012352.2:g.36865G>C , LRG_215:g.36865G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.505G>C MANE Select ENSP00000263735.4:p.Glu169Gln
ENST00000263735.8:c.505G>C ENSP00000263735.4:p.Glu169Gln
ENST00000405271.5:c.589G>C ENSP00000385476.1:p.Glu197Gln
ENST00000456133.5:c.589G>C ENSP00000410675.1:p.Glu197Gln
ENST00000490733.1:n.354G>C
NM_002354.2:c.505G>C , LRG_215t1:c.505G>C NP_002345.2:p.Glu169Gln
NM_002354.3:c.505G>C MANE Select NP_002345.2:p.Glu169Gln
Search 100 bp 5'
Search 100 bp 3'