Canonical Allele Identifier: CA1395153847
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1364681896

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462249G>A , CM000665.2:g.116462249G>A GRCh38
NC_000003.11:g.116181096G>A , CM000665.1:g.116181096G>A GRCh37
NC_000003.10:g.117663786G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.179-17294C>T ENSP00000418506.1:n.179-17294C>T