Canonical Allele Identifier: CA1052582836
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs138584640

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061173A>G , CM000665.2:g.117061173A>G GRCh38
NC_000003.11:g.116780020A>G , CM000665.1:g.116780020A>G GRCh37
NC_000003.10:g.118262710A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.34-51799T>C ENSP00000418506.1:n.34-51799T>C