Canonical Allele Identifier: CA897565999
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1411320483

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462113A>G , CM000665.2:g.116462113A>G GRCh38
NC_000003.11:g.116180960A>G , CM000665.1:g.116180960A>G GRCh37
NC_000003.10:g.117663650A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.179-17158T>C ENSP00000418506.1:n.179-17158T>C