Canonical Allele Identifier: CA1395153881
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462312T= , CM000665.2:g.116462312T= GRCh38
NC_000003.11:g.116181159T= , CM000665.1:g.116181159T= GRCh37
NC_000003.10:g.117663849T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.179-17357A= ENSP00000418506.1:n.179-17357A=