Canonical Allele Identifier: CA897565889
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs893187792
MyVariant Identifiers: chr3:g.116180576C>A (hg19) chr3:g.116461729C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461729C>A , CM000665.2:g.116461729C>A GRCh38
NC_000003.11:g.116180576C>A , CM000665.1:g.116180576C>A GRCh37
NC_000003.10:g.117663266C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16774G>T ENSP00000418506.1:n.179-16774G>T
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