Canonical Allele Identifier: CA817170002
Gene: MFSD4B-DT HGNC NCBI

Linked Data

dbSNP Id: rs1388492817
gnomAD v3: 6-111233566-T-C
gnomAD v4: 6-111233566-T-C
MyVariant Identifiers: chr6:g.111554769T>C (hg19) chr6:g.111233566T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233566T>C , CM000668.2:g.111233566T>C GRCh38
NC_000006.11:g.111554769T>C , CM000668.1:g.111554769T>C GRCh37
NC_000006.10:g.111661462T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001743806.1:n.348+433A>G
XR_001743807.1:n.154+433A>G
XR_001743808.1:n.348+433A>G
Search 100 bp 5'
Search 100 bp 3'