Canonical Allele Identifier: CA648537481
Gene: LSAMP HGNC NCBI

Linked Data

COSMIC: COSN21646001
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462040T>G , CM000665.2:g.116462040T>G GRCh38
NC_000003.11:g.116180887T>G , CM000665.1:g.116180887T>G GRCh37
NC_000003.10:g.117663577T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17085A>C ENSP00000418506.1:n.179-17085A>C
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