Canonical Allele Identifier: CA82071769
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs984898979
gnomAD v2: 3-116180643-G-T
gnomAD v3: 3-116461796-G-T
gnomAD v4: 3-116461796-G-T
MyVariant Identifiers: chr3:g.116180643G>T (hg19) chr3:g.116461796G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461796G>T , CM000665.2:g.116461796G>T GRCh38
NC_000003.11:g.116180643G>T , CM000665.1:g.116180643G>T GRCh37
NC_000003.10:g.117663333G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16841C>A ENSP00000418506.1:n.179-16841C>A
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