Canonical Allele Identifier: CA1395153415
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2049670920

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116461765_116461767del , CM000665.2:g.116461765_116461767del GRCh38
NC_000003.11:g.116180612_116180614del , CM000665.1:g.116180612_116180614del GRCh37
NC_000003.10:g.117663302_117663304del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-16806_179-16804del ENSP00000418506.1:n.179-16806_179-16804del