Canonical Allele Identifier: CA1584567013
Gene: SLC25A48 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135540896T= , CM000667.2:g.135540896T= GRCh38
NC_000005.9:g.134876586T= , CM000667.1:g.134876586T= GRCh37
NC_000005.8:g.134904485T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000698885.1:n.364+31140T=