Canonical Allele Identifier: CA631619920

Gene: NDUFA11

Linked Data

• dbSNP Id: rs1568433698
• gnomAD v2: 19-5903940-C-CA
• gnomAD v4: 19-5903929-C-CA
• MyVariant Identifiers: chr19:g.5903940_5903941insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5903930dup , CM000681.2:g.5903930dup	GRCh38
NC_000019.9:g.5903941dup , CM000681.1:g.5903941dup	GRCh37
NC_000019.8:g.5854941dup	NCBI36
NG_027808.1:g.5084dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000591160.1:n.77dup
NM_001193375.1:c.-222dup	NP_001180304.1:n.-222dup
NM_175614.4:c.-222dup	NP_783313.1:n.-222dup
NR_034166.2:n.84dup