Canonical Allele Identifier: CA82071783

Gene: LSAMP

Linked Data

• dbSNP Id: rs991569333
• gnomAD v2: 3-116180769-T-A
• gnomAD v3: 3-116461922-T-A
• gnomAD v4: 3-116461922-T-A
• MyVariant Identifiers: chr3:g.116180769T>A (hg19) ; chr3:g.116461922T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116461922T>A , CM000665.2:g.116461922T>A	GRCh38
NC_000003.11:g.116180769T>A , CM000665.1:g.116180769T>A	GRCh37
NC_000003.10:g.117663459T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-16967A>T	ENSP00000418506.1:n.179-16967A>T