Canonical Allele Identifier: CA31677484
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs553699163
gnomAD v2: 1-161184507-T-C
gnomAD v3: 1-161214717-T-C
gnomAD v4: 1-161214717-T-C
MyVariant Identifiers: chr1:g.161184507T>C (hg19) chr1:g.161214717T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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