Canonical Allele Identifier: CA545806395
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1370403981
gnomAD v2: 3-116180832-A-G
MyVariant Identifiers: chr3:g.116180832A>G (hg19) chr3:g.116461985A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461985A>G , CM000665.2:g.116461985A>G GRCh38
NC_000003.11:g.116180832A>G , CM000665.1:g.116180832A>G GRCh37
NC_000003.10:g.117663522A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17030T>C ENSP00000418506.1:n.179-17030T>C
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