Canonical Allele Identifier: CA897585793

Gene: LSAMP

Linked Data

• dbSNP Id: rs138584640
• gnomAD v3: 3-117061173-A-T
• gnomAD v4: 3-117061173-A-T
• MyVariant Identifiers: chr3:g.116780020A>T (hg19) ; chr3:g.117061173A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.117061173A>T , CM000665.2:g.117061173A>T	GRCh38
NC_000003.11:g.116780020A>T , CM000665.1:g.116780020A>T	GRCh37
NC_000003.10:g.118262710A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.34-51799T>A	ENSP00000418506.1:n.34-51799T>A