Canonical Allele Identifier: CA1093157431
Gene: MFSD4B-DT HGNC NCBI

Linked Data

dbSNP Id: rs1771158257

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233579T>C , CM000668.2:g.111233579T>C GRCh38
NC_000006.11:g.111554782T>C , CM000668.1:g.111554782T>C GRCh37
NC_000006.10:g.111661475T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001743806.1:n.348+420A>G
XR_001743807.1:n.154+420A>G
XR_001743808.1:n.348+420A>G