Canonical Allele Identifier: CA526610770
Gene: LCE3C HGNC NCBI

Linked Data

dbSNP Id: rs1282560510
gnomAD v2: 1-152537902-C-A
gnomAD v3: 1-152565426-C-A
gnomAD v4: 1-152565426-C-A
MyVariant Identifiers: chr1:g.152537902C>A (hg19) chr1:g.152565426C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152565426C>A , CM000663.2:g.152565426C>A GRCh38
NC_000001.10:g.152537902C>A , CM000663.1:g.152537902C>A GRCh37
NC_000001.9:g.150804526C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000617545.1:c.45-35365C>A ENSP00000482477.1:n.45-35365C>A
Search 100 bp 5'
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