Canonical Allele Identifier: CA82071827
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs554929126
gnomAD v3: 3-116462281-T-G
gnomAD v4: 3-116462281-T-G
MyVariant Identifiers: chr3:g.116181128T>G (hg19) chr3:g.116462281T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462281T>G , CM000665.2:g.116462281T>G GRCh38
NC_000003.11:g.116181128T>G , CM000665.1:g.116181128T>G GRCh37
NC_000003.10:g.117663818T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17326A>C ENSP00000418506.1:n.179-17326A>C
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