Canonical Allele Identifier: CA526875201
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1426091636
gnomAD v2: 1-161184503-CAG-C
gnomAD v3: 1-161214713-CAG-C
gnomAD v4: 1-161214713-CAG-C
MyVariant Identifiers: chr1:g.161184504_161184505del (hg19) chr1:g.161214714_161214715del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214715_161214716del , CM000663.2:g.161214715_161214716del GRCh38
NC_000001.10:g.161184505_161184506del , CM000663.1:g.161184505_161184506del GRCh37
NC_000001.9:g.159451129_159451130del NCBI36
NG_013352.1:g.20401_20402del
NG_029043.1:g.4419_4420del

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4774_4775del
ENST00000678492.1:n.4538_4539del
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