Canonical Allele Identifier: CA1395153353
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2049670232
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461710A>T , CM000665.2:g.116461710A>T GRCh38
NC_000003.11:g.116180557A>T , CM000665.1:g.116180557A>T GRCh37
NC_000003.10:g.117663247A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16755T>A ENSP00000418506.1:n.179-16755T>A
Search 100 bp 5'
Search 100 bp 3'