Canonical Allele Identifier: CA82144657

Gene: LSAMP

Linked Data

• dbSNP Id: rs757165888
• gnomAD v2: 3-116779964-C-G
• gnomAD v3: 3-117061117-C-G
• gnomAD v4: 3-117061117-C-G
• MyVariant Identifiers: chr3:g.116779964C>G (hg19) ; chr3:g.117061117C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.117061117C>G , CM000665.2:g.117061117C>G	GRCh38
NC_000003.11:g.116779964C>G , CM000665.1:g.116779964C>G	GRCh37
NC_000003.10:g.118262654C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000474851.1:c.34-51743G>C	ENSP00000418506.1:n.34-51743G>C