Canonical Allele Identifier: CA1654833067
Gene: MFSD4B-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233546G= , CM000668.2:g.111233546G= GRCh38
NC_000006.11:g.111554749G= , CM000668.1:g.111554749G= GRCh37
NC_000006.10:g.111661442G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743806.1:n.348+453C=
XR_001743807.1:n.154+453C=
XR_001743808.1:n.348+453C=