Canonical Allele Identifier: CA889406138

Gene: LCE3C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152520678G>T , CM000663.2:g.152520678G>T	GRCh38
NC_000001.10:g.152493154G>T , CM000663.1:g.152493154G>T	GRCh37
NC_000001.9:g.150759778G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617545.1:c.44+9100G>T	ENSP00000482477.1:n.44+9100G>T