Canonical Allele Identifier: CA1395153798
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462196T= , CM000665.2:g.116462196T= GRCh38
NC_000003.11:g.116181043T= , CM000665.1:g.116181043T= GRCh37
NC_000003.10:g.117663733T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.179-17241A= ENSP00000418506.1:n.179-17241A=