Canonical Allele Identifier: CA526610767

Gene: LCE3C

Linked Data

• dbSNP Id: rs1333903365
• gnomAD v2: 1-152537862-C-T
• gnomAD v3: 1-152565386-C-T
• gnomAD v4: 1-152565386-C-T
• MyVariant Identifiers: chr1:g.152537862C>T (hg19) ; chr1:g.152565386C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152565386C>T , CM000663.2:g.152565386C>T	GRCh38
NC_000001.10:g.152537862C>T , CM000663.1:g.152537862C>T	GRCh37
NC_000001.9:g.150804486C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000617545.1:c.45-35405C>T	ENSP00000482477.1:n.45-35405C>T