Canonical Allele Identifier: CA82071757

Gene: LSAMP

Linked Data

• dbSNP Id: rs947618838
• MyVariant Identifiers: chr3:g.116180556A>G (hg19) ; chr3:g.116461709A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116461709A>G , CM000665.2:g.116461709A>G	GRCh38
NC_000003.11:g.116180556A>G , CM000665.1:g.116180556A>G	GRCh37
NC_000003.10:g.117663246A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-16754T>C	ENSP00000418506.1:n.179-16754T>C