Canonical Allele Identifier: CA1395448093
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061201A= , CM000665.2:g.117061201A= GRCh38
NC_000003.11:g.116780048A= , CM000665.1:g.116780048A= GRCh37
NC_000003.10:g.118262738A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.34-51827T= ENSP00000418506.1:n.34-51827T=