Canonical Allele Identifier: CA31677473
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs572016427
gnomAD v3: 1-161214690-G-T
gnomAD v4: 1-161214690-G-T
MyVariant Identifiers: chr1:g.161184480G>T (hg19) chr1:g.161214690G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214690G>T , CM000663.2:g.161214690G>T GRCh38
NC_000001.10:g.161184480G>T , CM000663.1:g.161184480G>T GRCh37
NC_000001.9:g.159451104G>T NCBI36
NG_013352.1:g.20376G>T
NG_029043.1:g.4394G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4749G>T
ENST00000678492.1:n.4513G>T
Search 100 bp 5'
Search 100 bp 3'