Canonical Allele Identifier: CA1395448064
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061141G= , CM000665.2:g.117061141G= GRCh38
NC_000003.11:g.116779988G= , CM000665.1:g.116779988G= GRCh37
NC_000003.10:g.118262678G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.34-51767C= ENSP00000418506.1:n.34-51767C=