Canonical Allele Identifier: CA82071819
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs181287655

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462223C>T , CM000665.2:g.116462223C>T GRCh38
NC_000003.11:g.116181070C>T , CM000665.1:g.116181070C>T GRCh37
NC_000003.10:g.117663760C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.179-17268G>A ENSP00000418506.1:n.179-17268G>A