Canonical Allele Identifier: CA1666734589
Community Standard Title: NC_000006.12:g.137945548T=
Gene: SIMALR HGNC NCBI
LINC02865 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137945548T= , CM000668.2:g.137945548T= GRCh38
NC_000006.11:g.138266685T= , CM000668.1:g.138266685T= GRCh37
NC_000006.10:g.138308378T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_149097.1:n.132+121A= (SIMALR)
NR_174953.1:n.119+82T= (LINC02865)
XR_943061.1:n.314+121A= (SIMALR)