Canonical Allele Identifier: CA884020637

Gene: NDUFA11

Linked Data

• dbSNP Id: rs1228060662
• gnomAD v4: 19-5904009-C-T
• MyVariant Identifiers: chr19:g.5904020C>T (hg19) ; chr19:g.5904009C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5904009C>T , CM000681.2:g.5904009C>T	GRCh38
NC_000019.9:g.5904020C>T , CM000681.1:g.5904020C>T	GRCh37
NC_000019.8:g.5855020C>T	NCBI36
NG_027808.1:g.5005G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001193375.1:c.-301G>A	NP_001180304.1:n.-301G>A
NM_175614.4:c.-301G>A	NP_783313.1:n.-301G>A
NR_034166.2:n.5G>A