Canonical Allele Identifier: CA890190021
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs553699163
gnomAD v3: 1-161214717-T-G
gnomAD v4: 1-161214717-T-G
MyVariant Identifiers: chr1:g.161184507T>G (hg19) chr1:g.161214717T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214717T>G , CM000663.2:g.161214717T>G GRCh38
NC_000001.10:g.161184507T>G , CM000663.1:g.161184507T>G GRCh37
NC_000001.9:g.159451131T>G NCBI36
NG_013352.1:g.20403T>G
NG_029043.1:g.4421T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4776T>G
ENST00000678492.1:n.4540T>G
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