Canonical Allele Identifier: CA890190015
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1208919124
gnomAD v3: 1-161214699-CG-C
gnomAD v4: 1-161214699-CG-C
MyVariant Identifiers: chr1:g.161184490del (hg19) chr1:g.161214700del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214702del , CM000663.2:g.161214702del GRCh38
NC_000001.10:g.161184492del , CM000663.1:g.161184492del GRCh37
NC_000001.9:g.159451116del NCBI36
NG_013352.1:g.20388del
NG_029043.1:g.4406del

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4761del
ENST00000678492.1:n.4525del
Search 100 bp 5'
Search 100 bp 3'