Canonical Allele Identifier: CA82144667

Gene: LSAMP

Linked Data

• dbSNP Id: rs1016021786
• gnomAD v3: 3-117061201-A-G
• gnomAD v4: 3-117061201-A-G
• MyVariant Identifiers: chr3:g.116780048A>G (hg19) ; chr3:g.117061201A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.117061201A>G , CM000665.2:g.117061201A>G	GRCh38
NC_000003.11:g.116780048A>G , CM000665.1:g.116780048A>G	GRCh37
NC_000003.10:g.118262738A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000474851.1:c.34-51827T>C	ENSP00000418506.1:n.34-51827T>C