Canonical Allele Identifier: CA1395153688
Gene: LSAMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462038_116462039delinsCT , CM000665.2:g.116462038_116462039delinsCT GRCh38
NC_000003.11:g.116180885_116180886delinsCT , CM000665.1:g.116180885_116180886delinsCT GRCh37
NC_000003.10:g.117663575_117663576delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17084_179-17083delinsAG ENSP00000418506.1:n.179-17084_179-17083delinsAG
Search 100 bp 5'
Search 100 bp 3'