Canonical Allele Identifier: CA1654833074
Gene: MFSD4B-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233562A= , CM000668.2:g.111233562A= GRCh38
NC_000006.11:g.111554765A= , CM000668.1:g.111554765A= GRCh37
NC_000006.10:g.111661458A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743806.1:n.348+437T=
XR_001743807.1:n.154+437T=
XR_001743808.1:n.348+437T=