Canonical Allele Identifier: CA145237879
Gene: MFSD4B-DT HGNC NCBI

Linked Data

dbSNP Id: rs939760591

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233588T>C , CM000668.2:g.111233588T>C GRCh38
NC_000006.11:g.111554791T>C , CM000668.1:g.111554791T>C GRCh37
NC_000006.10:g.111661484T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743806.1:n.348+411A>G
XR_001743807.1:n.154+411A>G
XR_001743808.1:n.348+411A>G