Canonical Allele Identifier: CA1395153841
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462243G= , CM000665.2:g.116462243G= GRCh38
NC_000003.11:g.116181090G= , CM000665.1:g.116181090G= GRCh37
NC_000003.10:g.117663780G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17288C= ENSP00000418506.1:n.179-17288C=