Canonical Allele Identifier: CA897566077

Gene: LSAMP

Linked Data

• dbSNP Id: rs1447456921
• MyVariant Identifiers: chr3:g.116181130_116181131insT (hg19) ; chr3:g.116462283_116462284insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116462288dup , CM000665.2:g.116462288dup	GRCh38
NC_000003.11:g.116181135dup , CM000665.1:g.116181135dup	GRCh37
NC_000003.10:g.117663825dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-17329dup	ENSP00000418506.1:n.179-17329dup