Canonical Allele Identifier: CA817170017
Gene: MFSD4B-DT HGNC NCBI

Linked Data

dbSNP Id: rs1425339497
MyVariant Identifiers: chr6:g.111554792T>C (hg19) chr6:g.111233589T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233589T>C , CM000668.2:g.111233589T>C GRCh38
NC_000006.11:g.111554792T>C , CM000668.1:g.111554792T>C GRCh37
NC_000006.10:g.111661485T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001743806.1:n.348+410A>G
XR_001743807.1:n.154+410A>G
XR_001743808.1:n.348+410A>G
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