Canonical Allele Identifier: CA897585802
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1444796778
gnomAD v3: 3-117061182-T-C
gnomAD v4: 3-117061182-T-C
MyVariant Identifiers: chr3:g.116780029T>C (hg19) chr3:g.117061182T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061182T>C , CM000665.2:g.117061182T>C GRCh38
NC_000003.11:g.116780029T>C , CM000665.1:g.116780029T>C GRCh37
NC_000003.10:g.118262719T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.34-51808A>G ENSP00000418506.1:n.34-51808A>G
Search 100 bp 5'
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