Canonical Allele Identifier: CA890190000
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1406886950
gnomAD v3: 1-161214649-G-A
gnomAD v4: 1-161214649-G-A
MyVariant Identifiers: chr1:g.161184439G>A (hg19) chr1:g.161214649G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214649G>A , CM000663.2:g.161214649G>A GRCh38
NC_000001.10:g.161184439G>A , CM000663.1:g.161184439G>A GRCh37
NC_000001.9:g.159451063G>A NCBI36
NG_013352.1:g.20335G>A
NG_029043.1:g.4353G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4708G>A
ENST00000678492.1:n.4472G>A
Search 100 bp 5'
Search 100 bp 3'