Canonical Allele Identifier: CA1654833079
Gene: MFSD4B-DT HGNC NCBI

Linked Data

dbSNP Id: rs1771158090

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233572A>C , CM000668.2:g.111233572A>C GRCh38
NC_000006.11:g.111554775A>C , CM000668.1:g.111554775A>C GRCh37
NC_000006.10:g.111661468A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743806.1:n.348+427T>G
XR_001743807.1:n.154+427T>G
XR_001743808.1:n.348+427T>G