Canonical Allele Identifier: CA1395153832
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462219T= , CM000665.2:g.116462219T= GRCh38
NC_000003.11:g.116181066T= , CM000665.1:g.116181066T= GRCh37
NC_000003.10:g.117663756T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.179-17264A= ENSP00000418506.1:n.179-17264A=