Canonical Allele Identifier: CA545806408

Gene: LSAMP

Linked Data

• dbSNP Id: rs1215123517
• gnomAD v2: 3-116181145-A-G
• gnomAD v3: 3-116462298-A-G
• gnomAD v4: 3-116462298-A-G
• MyVariant Identifiers: chr3:g.116181145A>G (hg19) ; chr3:g.116462298A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116462298A>G , CM000665.2:g.116462298A>G	GRCh38
NC_000003.11:g.116181145A>G , CM000665.1:g.116181145A>G	GRCh37
NC_000003.10:g.117663835A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-17343T>C	ENSP00000418506.1:n.179-17343T>C