Canonical Allele Identifier: CA884020507
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs1221813450
MyVariant Identifiers: chr19:g.5903850A>T (hg19) chr19:g.5903839A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903839A>T , CM000681.2:g.5903839A>T GRCh38
NC_000019.9:g.5903850A>T , CM000681.1:g.5903850A>T GRCh37
NC_000019.8:g.5854850A>T NCBI36
NG_027808.1:g.5175T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.168T>A
NM_001193375.1:c.-131T>A NP_001180304.1:n.-131T>A
NM_175614.4:c.-131T>A NP_783313.1:n.-131T>A
NR_034166.2:n.175T>A
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