Canonical Allele Identifier: CA1395153558
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461903C= , CM000665.2:g.116461903C= GRCh38
NC_000003.11:g.116180750C= , CM000665.1:g.116180750C= GRCh37
NC_000003.10:g.117663440C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16948G= ENSP00000418506.1:n.179-16948G=