Canonical Allele Identifier: CA2500737170
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462135G>T , CM000665.2:g.116462135G>T GRCh38
NC_000003.11:g.116180982G>T , CM000665.1:g.116180982G>T GRCh37
NC_000003.10:g.117663672G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.179-17180C>A ENSP00000418506.1:n.179-17180C>A