Canonical Allele Identifier: CA545806389
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1211293569
gnomAD v2: 3-116180624-TA-T
gnomAD v3: 3-116461777-TA-T
gnomAD v4: 3-116461777-TA-T
MyVariant Identifiers: chr3:g.116180625del (hg19) chr3:g.116461778del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461781del , CM000665.2:g.116461781del GRCh38
NC_000003.11:g.116180628del , CM000665.1:g.116180628del GRCh37
NC_000003.10:g.117663318del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16823del ENSP00000418506.1:n.179-16823del
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