Canonical Allele Identifier: CA1395448084
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1576188127

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061176T>A , CM000665.2:g.117061176T>A GRCh38
NC_000003.11:g.116780023T>A , CM000665.1:g.116780023T>A GRCh37
NC_000003.10:g.118262713T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.34-51802A>T ENSP00000418506.1:n.34-51802A>T