Canonical Allele Identifier: CA1395153381
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461744C= , CM000665.2:g.116461744C= GRCh38
NC_000003.11:g.116180591C= , CM000665.1:g.116180591C= GRCh37
NC_000003.10:g.117663281C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16789G= ENSP00000418506.1:n.179-16789G=