Canonical Allele Identifier: CA1052544698
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1576237513

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462246G>A , CM000665.2:g.116462246G>A GRCh38
NC_000003.11:g.116181093G>A , CM000665.1:g.116181093G>A GRCh37
NC_000003.10:g.117663783G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17291C>T ENSP00000418506.1:n.179-17291C>T