Canonical Allele Identifier: CA1654833075
Gene: MFSD4B-DT HGNC NCBI

Linked Data

dbSNP Id: rs1771157903

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XR_001743806.1:n.348+437T>C
XR_001743807.1:n.154+437T>C
XR_001743808.1:n.348+437T>C