Canonical Allele Identifier: CA526610769

Gene: LCE3C

Linked Data

• dbSNP Id: rs1244087369
• gnomAD v2: 1-152537868-G-T
• gnomAD v3: 1-152565392-G-T
• gnomAD v4: 1-152565392-G-T
• MyVariant Identifiers: chr1:g.152537868G>T (hg19) ; chr1:g.152565392G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152565392G>T , CM000663.2:g.152565392G>T	GRCh38
NC_000001.10:g.152537868G>T , CM000663.1:g.152537868G>T	GRCh37
NC_000001.9:g.150804492G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000617545.1:c.45-35399G>T	ENSP00000482477.1:n.45-35399G>T