Canonical Allele Identifier: CA2512262496
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462248T>C , CM000665.2:g.116462248T>C GRCh38
NC_000003.11:g.116181095T>C , CM000665.1:g.116181095T>C GRCh37
NC_000003.10:g.117663785T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17293A>G ENSP00000418506.1:n.179-17293A>G