Canonical Allele Identifier: CA82071776
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs932994721
gnomAD v3: 3-116461863-C-T
gnomAD v4: 3-116461863-C-T
MyVariant Identifiers: chr3:g.116180710C>T (hg19) chr3:g.116461863C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461863C>T , CM000665.2:g.116461863C>T GRCh38
NC_000003.11:g.116180710C>T , CM000665.1:g.116180710C>T GRCh37
NC_000003.10:g.117663400C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16908G>A ENSP00000418506.1:n.179-16908G>A
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