Canonical Allele Identifier: CA304700040

Gene: NDUFA11

Linked Data

• dbSNP Id: rs996493424
• gnomAD v2: 19-5903924-G-A
• gnomAD v4: 19-5903913-G-A
• MyVariant Identifiers: chr19:g.5903924G>A (hg19) ; chr19:g.5903913G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5903913G>A , CM000681.2:g.5903913G>A	GRCh38
NC_000019.9:g.5903924G>A , CM000681.1:g.5903924G>A	GRCh37
NC_000019.8:g.5854924G>A	NCBI36
NG_027808.1:g.5101C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000591160.1:n.94C>T
NM_001193375.1:c.-205C>T	NP_001180304.1:n.-205C>T
NM_175614.4:c.-205C>T	NP_783313.1:n.-205C>T
NR_034166.2:n.101C>T