Canonical Allele Identifier: CA82071759

Gene: LSAMP

Linked Data

• dbSNP Id: rs893187792
• gnomAD v2: 3-116180576-C-T
• gnomAD v3: 3-116461729-C-T
• gnomAD v4: 3-116461729-C-T
• MyVariant Identifiers: chr3:g.116180576C>T (hg19) ; chr3:g.116461729C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116461729C>T , CM000665.2:g.116461729C>T	GRCh38
NC_000003.11:g.116180576C>T , CM000665.1:g.116180576C>T	GRCh37
NC_000003.10:g.117663266C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-16774G>A	ENSP00000418506.1:n.179-16774G>A