Canonical Allele Identifier: CA1395153673
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2049673063

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462020G>T , CM000665.2:g.116462020G>T GRCh38
NC_000003.11:g.116180867G>T , CM000665.1:g.116180867G>T GRCh37
NC_000003.10:g.117663557G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17065C>A ENSP00000418506.1:n.179-17065C>A