Canonical Allele Identifier: CA889428352
Gene: LCE3C HGNC NCBI

Linked Data

dbSNP Id: rs1260275946
MyVariant Identifiers: chr1:g.152537875C>T (hg19) chr1:g.152565399C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152565399C>T , CM000663.2:g.152565399C>T GRCh38
NC_000001.10:g.152537875C>T , CM000663.1:g.152537875C>T GRCh37
NC_000001.9:g.150804499C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000617545.1:c.45-35392C>T ENSP00000482477.1:n.45-35392C>T
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