Canonical Allele Identifier: CA2703644033
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1003569673
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461753C>T , CM000665.2:g.116461753C>T GRCh38
NC_000003.11:g.116180600C>T , CM000665.1:g.116180600C>T GRCh37
NC_000003.10:g.117663290C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16798G>A ENSP00000418506.1:n.179-16798G>A
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