Canonical Allele Identifier: CA82144663
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs756465365
gnomAD v2: 3-116780011-G-T
gnomAD v3: 3-117061164-G-T
gnomAD v4: 3-117061164-G-T
MyVariant Identifiers: chr3:g.116780011G>T (hg19) chr3:g.117061164G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061164G>T , CM000665.2:g.117061164G>T GRCh38
NC_000003.11:g.116780011G>T , CM000665.1:g.116780011G>T GRCh37
NC_000003.10:g.118262701G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.34-51790C>A ENSP00000418506.1:n.34-51790C>A
Search 100 bp 5'
Search 100 bp 3'