Canonical Allele Identifier: CA897565929

Gene: LSAMP

Linked Data

• dbSNP Id: rs1400829497
• gnomAD v3: 3-116461862-A-G
• gnomAD v4: 3-116461862-A-G
• MyVariant Identifiers: chr3:g.116180709A>G (hg19) ; chr3:g.116461862A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116461862A>G , CM000665.2:g.116461862A>G	GRCh38
NC_000003.11:g.116180709A>G , CM000665.1:g.116180709A>G	GRCh37
NC_000003.10:g.117663399A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-16907T>C	ENSP00000418506.1:n.179-16907T>C