Canonical Allele Identifier: CA890190001
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1388309022
MyVariant Identifiers: chr1:g.161184447T>G (hg19) chr1:g.161214657T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214657T>G , CM000663.2:g.161214657T>G GRCh38
NC_000001.10:g.161184447T>G , CM000663.1:g.161184447T>G GRCh37
NC_000001.9:g.159451071T>G NCBI36
NG_013352.1:g.20343T>G
NG_029043.1:g.4361T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4716T>G
ENST00000678492.1:n.4480T>G
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