Canonical Allele Identifier: CA2603490047
Gene: LSAMP HGNC NCBI

Linked Data

gnomAD v3: 3-117061241-G-A
gnomAD v4: 3-117061241-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061241G>A , CM000665.2:g.117061241G>A GRCh38
NC_000003.11:g.116780088G>A , CM000665.1:g.116780088G>A GRCh37
NC_000003.10:g.118262778G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.34-51867C>T ENSP00000418506.1:n.34-51867C>T
Search 100 bp 5'
Search 100 bp 3'