Canonical Allele Identifier: CA545806396

Gene: LSAMP

Linked Data

• dbSNP Id: rs1220252976
• gnomAD v2: 3-116180833-TA-T
• gnomAD v3: 3-116461986-TA-T
• gnomAD v4: 3-116461986-TA-T
• MyVariant Identifiers: chr3:g.116180834del (hg19) ; chr3:g.116461987del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116461987del , CM000665.2:g.116461987del	GRCh38
NC_000003.11:g.116180834del , CM000665.1:g.116180834del	GRCh37
NC_000003.10:g.117663524del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-17032del	ENSP00000418506.1:n.179-17032del