Canonical Allele Identifier: CA31677479
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs536878491
gnomAD v2: 1-161184490-G-A
gnomAD v3: 1-161214700-G-A
gnomAD v4: 1-161214700-G-A
MyVariant Identifiers: chr1:g.161184490G>A (hg19) chr1:g.161214700G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214700G>A , CM000663.2:g.161214700G>A GRCh38
NC_000001.10:g.161184490G>A , CM000663.1:g.161184490G>A GRCh37
NC_000001.9:g.159451114G>A NCBI36
NG_013352.1:g.20386G>A
NG_029043.1:g.4404G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4759G>A
ENST00000678492.1:n.4523G>A
Search 100 bp 5'
Search 100 bp 3'