Canonical Allele Identifier: CA890190004
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1381045584
gnomAD v3: 1-161214677-G-A
gnomAD v4: 1-161214677-G-A
MyVariant Identifiers: chr1:g.161184467G>A (hg19) chr1:g.161214677G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214677G>A , CM000663.2:g.161214677G>A GRCh38
NC_000001.10:g.161184467G>A , CM000663.1:g.161184467G>A GRCh37
NC_000001.9:g.159451091G>A NCBI36
NG_013352.1:g.20363G>A
NG_029043.1:g.4381G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4736G>A
ENST00000678492.1:n.4500G>A
Search 100 bp 5'
Search 100 bp 3'