Canonical Allele Identifier: CA897565944

Gene: LSAMP

Linked Data

• dbSNP Id: rs1486572678
• MyVariant Identifiers: chr3:g.116180783del (hg19) ; chr3:g.116461936del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116461938del , CM000665.2:g.116461938del	GRCh38
NC_000003.11:g.116180785del , CM000665.1:g.116180785del	GRCh37
NC_000003.10:g.117663475del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-16981del	ENSP00000418506.1:n.179-16981del