Canonical Allele Identifier: CA420884664

Gene: LCE3C

Linked Data

• dbSNP Id: rs1434361293
• gnomAD v3: 1-152565445-T-G
• gnomAD v4: 1-152565445-T-G
• MyVariant Identifiers: chr1:g.152537921T>G (hg19) ; chr1:g.152565445T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152565445T>G , CM000663.2:g.152565445T>G	GRCh38
NC_000001.10:g.152537921T>G , CM000663.1:g.152537921T>G	GRCh37
NC_000001.9:g.150804545T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617545.1:c.45-35346T>G	ENSP00000482477.1:n.45-35346T>G