Canonical Allele Identifier: CA1052544714
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2049675201

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462297A>G , CM000665.2:g.116462297A>G GRCh38
NC_000003.11:g.116181144A>G , CM000665.1:g.116181144A>G GRCh37
NC_000003.10:g.117663834A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17342T>C ENSP00000418506.1:n.179-17342T>C