Canonical Allele Identifier: CA648537483
Gene: LSAMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462311C>A , CM000665.2:g.116462311C>A GRCh38
NC_000003.11:g.116181158C>A , CM000665.1:g.116181158C>A GRCh37
NC_000003.10:g.117663848C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17356G>T ENSP00000418506.1:n.179-17356G>T