Canonical Allele Identifier: CA545806399
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1248486296

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462051G>A , CM000665.2:g.116462051G>A GRCh38
NC_000003.11:g.116180898G>A , CM000665.1:g.116180898G>A GRCh37
NC_000003.10:g.117663588G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17096C>T ENSP00000418506.1:n.179-17096C>T