Canonical Allele Identifier: CA884020614

Gene: NDUFA11

Linked Data

• dbSNP Id: rs1487717986
• MyVariant Identifiers: chr19:g.5903995T>G (hg19) ; chr19:g.5903984T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5903984T>G , CM000681.2:g.5903984T>G	GRCh38
NC_000019.9:g.5903995T>G , CM000681.1:g.5903995T>G	GRCh37
NC_000019.8:g.5854995T>G	NCBI36
NG_027808.1:g.5030A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000591160.1:n.23A>C
NM_001193375.1:c.-276A>C	NP_001180304.1:n.-276A>C
NM_175614.4:c.-276A>C	NP_783313.1:n.-276A>C
NR_034166.2:n.30A>C