Canonical Allele Identifier: CA1395153689
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2049673169
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462041del , CM000665.2:g.116462041del GRCh38
NC_000003.11:g.116180888del , CM000665.1:g.116180888del GRCh37
NC_000003.10:g.117663578del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17084del ENSP00000418506.1:n.179-17084del
Search 100 bp 5'
Search 100 bp 3'