Canonical Allele Identifier: CA1052544627

Gene: LSAMP

Linked Data

• dbSNP Id: rs2049670244
• gnomAD v3: 3-116461712-A-T
• gnomAD v4: 3-116461712-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116461712A>T , CM000665.2:g.116461712A>T	GRCh38
NC_000003.11:g.116180559A>T , CM000665.1:g.116180559A>T	GRCh37
NC_000003.10:g.117663249A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-16757T>A	ENSP00000418506.1:n.179-16757T>A