Canonical Allele Identifier: CA897565899

Gene: LSAMP

Linked Data

• dbSNP Id: rs890174864
• gnomAD v3: 3-116461757-C-A
• gnomAD v4: 3-116461757-C-A
• MyVariant Identifiers: chr3:g.116180604C>A (hg19) ; chr3:g.116461757C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116461757C>A , CM000665.2:g.116461757C>A	GRCh38
NC_000003.11:g.116180604C>A , CM000665.1:g.116180604C>A	GRCh37
NC_000003.10:g.117663294C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-16802G>T	ENSP00000418506.1:n.179-16802G>T