Canonical Allele Identifier: CA2603448781
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2107909232

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462102C>A , CM000665.2:g.116462102C>A GRCh38
NC_000003.11:g.116180949C>A , CM000665.1:g.116180949C>A GRCh37
NC_000003.10:g.117663639C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.179-17147G>T ENSP00000418506.1:n.179-17147G>T