Canonical Allele Identifier: CA145237865

Gene: MFSD4B-DT

Linked Data

• dbSNP Id: rs370724512
• gnomAD v2: 6-111554766-C-T
• gnomAD v3: 6-111233563-C-T
• gnomAD v4: 6-111233563-C-T
• MyVariant Identifiers: chr6:g.111554766C>T (hg19) ; chr6:g.111233563C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111233563C>T , CM000668.2:g.111233563C>T	GRCh38
NC_000006.11:g.111554766C>T , CM000668.1:g.111554766C>T	GRCh37
NC_000006.10:g.111661459C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743806.1:n.348+436G>A
XR_001743807.1:n.154+436G>A
XR_001743808.1:n.348+436G>A