Canonical Allele Identifier: CA817170010
Gene: MFSD4B-DT HGNC NCBI

Linked Data

dbSNP Id: rs1169773312
gnomAD v3: 6-111233583-C-T
gnomAD v4: 6-111233583-C-T
MyVariant Identifiers: chr6:g.111554786C>T (hg19) chr6:g.111233583C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233583C>T , CM000668.2:g.111233583C>T GRCh38
NC_000006.11:g.111554786C>T , CM000668.1:g.111554786C>T GRCh37
NC_000006.10:g.111661479C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743806.1:n.348+416G>A
XR_001743807.1:n.154+416G>A
XR_001743808.1:n.348+416G>A
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