Canonical Allele Identifier: CA1395153450
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2049671273

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461792G>C , CM000665.2:g.116461792G>C GRCh38
NC_000003.11:g.116180639G>C , CM000665.1:g.116180639G>C GRCh37
NC_000003.10:g.117663329G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16837C>G ENSP00000418506.1:n.179-16837C>G