Canonical Allele Identifier: CA15461157
Gene: MFSD4B-DT HGNC NCBI

Linked Data

dbSNP Id: rs6901004

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233619C>G , CM000668.2:g.111233619C>G GRCh38
NC_000006.11:g.111554822C>G , CM000668.1:g.111554822C>G GRCh37
NC_000006.10:g.111661515C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001743806.1:n.348+380G>C
XR_001743807.1:n.154+380G>C
XR_001743808.1:n.348+380G>C