Canonical Allele Identifier: CA2587725803
Gene: NDUFA11 HGNC NCBI

Linked Data

gnomAD v4: 19-5903915-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903915A>C , CM000681.2:g.5903915A>C GRCh38
NC_000019.9:g.5903926A>C , CM000681.1:g.5903926A>C GRCh37
NC_000019.8:g.5854926A>C NCBI36
NG_027808.1:g.5099T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.92T>G
NM_001193375.1:c.-207T>G NP_001180304.1:n.-207T>G
NM_175614.4:c.-207T>G NP_783313.1:n.-207T>G
NR_034166.2:n.99T>G