Canonical Allele Identifier: CA229042118

Gene: FDX1

Linked Data

• dbSNP Id: rs944094053
• gnomAD v3: 11-110460832-T-C
• gnomAD v4: 11-110460832-T-C
• MyVariant Identifiers: chr11:g.110331556T>C (hg19) ; chr11:g.110460832T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110460832T>C , CM000673.2:g.110460832T>C	GRCh38
NC_000011.9:g.110331556T>C , CM000673.1:g.110331556T>C	GRCh37
NC_000011.8:g.109836766T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260270.3:c.441-1522T>C MANE Select	ENSP00000260270.2:n.441-1522T>C
ENST00000260270.2:c.441-1522T>C	ENSP00000260270.2:n.441-1522T>C
NM_004109.4:c.441-1522T>C	NP_004100.1:n.441-1522T>C
NM_004109.5:c.441-1522T>C MANE Select	NP_004100.1:n.441-1522T>C