Canonical Allele Identifier: CA82071811
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs959228026
gnomAD v2: 3-116181013-A-C
gnomAD v3: 3-116462166-A-C
gnomAD v4: 3-116462166-A-C
MyVariant Identifiers: chr3:g.116181013A>C (hg19) chr3:g.116462166A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462166A>C , CM000665.2:g.116462166A>C GRCh38
NC_000003.11:g.116181013A>C , CM000665.1:g.116181013A>C GRCh37
NC_000003.10:g.117663703A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17211T>G ENSP00000418506.1:n.179-17211T>G
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