Canonical Allele Identifier: CA1654833089
Gene: MFSD4B-DT HGNC NCBI

Linked Data

dbSNP Id: rs1771158576
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111233595C>T , CM000668.2:g.111233595C>T GRCh38
NC_000006.11:g.111554798C>T , CM000668.1:g.111554798C>T GRCh37
NC_000006.10:g.111661491C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001743806.1:n.348+404G>A
XR_001743807.1:n.154+404G>A
XR_001743808.1:n.348+404G>A
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