Canonical Allele Identifier: CA1395153521
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461867G= , CM000665.2:g.116461867G= GRCh38
NC_000003.11:g.116180714G= , CM000665.1:g.116180714G= GRCh37
NC_000003.10:g.117663404G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16912C= ENSP00000418506.1:n.179-16912C=