Canonical Allele Identifier: CA601961310

Gene: FDX1

Linked Data

• dbSNP Id: rs1418758419
• gnomAD v2: 11-110331557-G-C
• gnomAD v3: 11-110460833-G-C
• gnomAD v4: 11-110460833-G-C
• MyVariant Identifiers: chr11:g.110331557G>C (hg19) ; chr11:g.110460833G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110460833G>C , CM000673.2:g.110460833G>C	GRCh38
NC_000011.9:g.110331557G>C , CM000673.1:g.110331557G>C	GRCh37
NC_000011.8:g.109836767G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260270.3:c.441-1521G>C MANE Select	ENSP00000260270.2:n.441-1521G>C
ENST00000260270.2:c.441-1521G>C	ENSP00000260270.2:n.441-1521G>C
NM_004109.4:c.441-1521G>C	NP_004100.1:n.441-1521G>C
NM_004109.5:c.441-1521G>C MANE Select	NP_004100.1:n.441-1521G>C