Canonical Allele Identifier: CA897566084

Gene: LSAMP

Linked Data

• dbSNP Id: rs1486249221
• gnomAD v3: 3-116462303-G-T
• gnomAD v4: 3-116462303-G-T
• MyVariant Identifiers: chr3:g.116181150G>T (hg19) ; chr3:g.116462303G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116462303G>T , CM000665.2:g.116462303G>T	GRCh38
NC_000003.11:g.116181150G>T , CM000665.1:g.116181150G>T	GRCh37
NC_000003.10:g.117663840G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-17348C>A	ENSP00000418506.1:n.179-17348C>A