Canonical Allele Identifier: CA897585702

Gene: LSAMP

Linked Data

• dbSNP Id: rs1330563227
• gnomAD v3: 3-117061100-T-A
• gnomAD v4: 3-117061100-T-A
• MyVariant Identifiers: chr3:g.116779947T>A (hg19) ; chr3:g.117061100T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.117061100T>A , CM000665.2:g.117061100T>A	GRCh38
NC_000003.11:g.116779947T>A , CM000665.1:g.116779947T>A	GRCh37
NC_000003.10:g.118262637T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.34-51726A>T	ENSP00000418506.1:n.34-51726A>T