Canonical Allele Identifier: CA897565917

Gene: LSAMP

Linked Data

• dbSNP Id: rs1295053545
• gnomAD v3: 3-116461838-TC-T
• gnomAD v4: 3-116461838-TC-T
• MyVariant Identifiers: chr3:g.116180686del (hg19) ; chr3:g.116461839del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116461839del , CM000665.2:g.116461839del	GRCh38
NC_000003.11:g.116180686del , CM000665.1:g.116180686del	GRCh37
NC_000003.10:g.117663376del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-16884del	ENSP00000418506.1:n.179-16884del