Canonical Allele Identifier: CA897566072

Gene: LSAMP

Linked Data

• dbSNP Id: rs1333669292
• MyVariant Identifiers: chr3:g.116181120T>A (hg19) ; chr3:g.116462273T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116462273T>A , CM000665.2:g.116462273T>A	GRCh38
NC_000003.11:g.116181120T>A , CM000665.1:g.116181120T>A	GRCh37
NC_000003.10:g.117663810T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-17318A>T	ENSP00000418506.1:n.179-17318A>T