Canonical Allele Identifier: CA631619865
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs1278737086
gnomAD v2: 19-5903844-C-G
gnomAD v4: 19-5903833-C-G
MyVariant Identifiers: chr19:g.5903844C>G (hg19) chr19:g.5903833C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903833C>G , CM000681.2:g.5903833C>G GRCh38
NC_000019.9:g.5903844C>G , CM000681.1:g.5903844C>G GRCh37
NC_000019.8:g.5854844C>G NCBI36
NG_027808.1:g.5181G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.174G>C
NM_001193375.1:c.-125G>C NP_001180304.1:n.-125G>C
NM_175614.4:c.-125G>C NP_783313.1:n.-125G>C
NR_034166.2:n.181G>C
Search 100 bp 5'
Search 100 bp 3'