Canonical Allele Identifier: CA1584567033
Gene: SLC25A48 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135540941A= , CM000667.2:g.135540941A= GRCh38
NC_000005.9:g.134876631A= , CM000667.1:g.134876631A= GRCh37
NC_000005.8:g.134904530A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000698885.1:n.364+31185A=