Canonical Allele Identifier: CA2703664264
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1374955628

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461903C>A , CM000665.2:g.116461903C>A GRCh38
NC_000003.11:g.116180750C>A , CM000665.1:g.116180750C>A GRCh37
NC_000003.10:g.117663440C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16948G>T ENSP00000418506.1:n.179-16948G>T