Canonical Allele Identifier: CA1395153863
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2049675036

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462277_116462278insTTAGAAGGT , CM000665.2:g.116462277_116462278insTTAGAAGGT GRCh38
NC_000003.11:g.116181124_116181125insTTAGAAGGT , CM000665.1:g.116181124_116181125insTTAGAAGGT GRCh37
NC_000003.10:g.117663814_117663815insTTAGAAGGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17323_179-17322insACCTTCTAA ENSP00000418506.1:n.179-17323_179-17322insACCTTCTAA