Canonical Allele Identifier: CA31677476
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs537594761
gnomAD v3: 1-161214696-T-C
gnomAD v4: 1-161214696-T-C
MyVariant Identifiers: chr1:g.161184486T>C (hg19) chr1:g.161214696T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214696T>C , CM000663.2:g.161214696T>C GRCh38
NC_000001.10:g.161184486T>C , CM000663.1:g.161184486T>C GRCh37
NC_000001.9:g.159451110T>C NCBI36
NG_013352.1:g.20382T>C
NG_029043.1:g.4400T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4755T>C
ENST00000678492.1:n.4519T>C
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