Canonical Allele Identifier: CA889428350
Gene: LCE3C HGNC NCBI

Linked Data

dbSNP Id: rs1448758871
MyVariant Identifiers: chr1:g.152537871T>C (hg19) chr1:g.152565395T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152565395T>C , CM000663.2:g.152565395T>C GRCh38
NC_000001.10:g.152537871T>C , CM000663.1:g.152537871T>C GRCh37
NC_000001.9:g.150804495T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000617545.1:c.45-35396T>C ENSP00000482477.1:n.45-35396T>C
Search 100 bp 5'
Search 100 bp 3'