Canonical Allele Identifier: CA2758032206
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462087T>G , CM000665.2:g.116462087T>G GRCh38
NC_000003.11:g.116180934T>G , CM000665.1:g.116180934T>G GRCh37
NC_000003.10:g.117663624T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17132A>C ENSP00000418506.1:n.179-17132A>C