Canonical Allele Identifier: CA1654833062
Gene: MFSD4B-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233533T= , CM000668.2:g.111233533T= GRCh38
NC_000006.11:g.111554736T= , CM000668.1:g.111554736T= GRCh37
NC_000006.10:g.111661429T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743806.1:n.348+466A=
XR_001743807.1:n.154+466A=
XR_001743808.1:n.348+466A=