Canonical Allele Identifier: CA897585770

Gene: LSAMP

Linked Data

• dbSNP Id: rs1246970130
• MyVariant Identifiers: chr3:g.116780009T>G (hg19) ; chr3:g.117061162T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.117061162T>G , CM000665.2:g.117061162T>G	GRCh38
NC_000003.11:g.116780009T>G , CM000665.1:g.116780009T>G	GRCh37
NC_000003.10:g.118262699T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.34-51788A>C	ENSP00000418506.1:n.34-51788A>C