Canonical Allele Identifier: CA1052544651
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2049672373
gnomAD v3: 3-116461937-G-C
gnomAD v4: 3-116461937-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461937G>C , CM000665.2:g.116461937G>C GRCh38
NC_000003.11:g.116180784G>C , CM000665.1:g.116180784G>C GRCh37
NC_000003.10:g.117663474G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16982C>G ENSP00000418506.1:n.179-16982C>G
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