Canonical Allele Identifier: CA1007776728
Gene: LCE3C HGNC NCBI

Linked Data

dbSNP Id: rs1659892229
gnomAD v3: 1-152565381-A-G
gnomAD v4: 1-152565381-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152565381A>G , CM000663.2:g.152565381A>G GRCh38
NC_000001.10:g.152537857A>G , CM000663.1:g.152537857A>G GRCh37
NC_000001.9:g.150804481A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000617545.1:c.45-35410A>G ENSP00000482477.1:n.45-35410A>G
Search 100 bp 5'
Search 100 bp 3'