Canonical Allele Identifier: CA1584567010
Gene: SLC25A48 HGNC NCBI

Linked Data

dbSNP Id: rs1750604617

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135540885G>A , CM000667.2:g.135540885G>A GRCh38
NC_000005.9:g.134876575G>A , CM000667.1:g.134876575G>A GRCh37
NC_000005.8:g.134904474G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000698885.1:n.364+31129G>A