Canonical Allele Identifier: CA889428292

Gene: LCE3C

Linked Data

• dbSNP Id: rs1238804021
• gnomAD v2: 1-152537791-A-G
• gnomAD v3: 1-152565315-A-G
• gnomAD v4: 1-152565315-A-G
• MyVariant Identifiers: chr1:g.152537791A>G (hg19) ; chr1:g.152565315A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152565315A>G , CM000663.2:g.152565315A>G	GRCh38
NC_000001.10:g.152537791A>G , CM000663.1:g.152537791A>G	GRCh37
NC_000001.9:g.150804415A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617545.1:c.45-35476A>G	ENSP00000482477.1:n.45-35476A>G