Canonical Allele Identifier: CA30625885

Gene: LCE3C

Linked Data

• dbSNP Id: rs141443165
• gnomAD v2: 1-152537854-T-A
• gnomAD v3: 1-152565378-T-A
• gnomAD v4: 1-152565378-T-A
• MyVariant Identifiers: chr1:g.152537854T>A (hg19) ; chr1:g.152565378T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152565378T>A , CM000663.2:g.152565378T>A	GRCh38
NC_000001.10:g.152537854T>A , CM000663.1:g.152537854T>A	GRCh37
NC_000001.9:g.150804478T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000617545.1:c.45-35413T>A	ENSP00000482477.1:n.45-35413T>A