Canonical Allele Identifier: CA2703821047
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2107491530
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061253A>T , CM000665.2:g.117061253A>T GRCh38
NC_000003.11:g.116780100A>T , CM000665.1:g.116780100A>T GRCh37
NC_000003.10:g.118262790A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.34-51879T>A ENSP00000418506.1:n.34-51879T>A
Search 100 bp 5'
Search 100 bp 3'