Canonical Allele Identifier: CA31677454
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs993291579
MyVariant Identifiers: chr1:g.161184450G>A (hg19) chr1:g.161214660G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214660G>A , CM000663.2:g.161214660G>A GRCh38
NC_000001.10:g.161184450G>A , CM000663.1:g.161184450G>A GRCh37
NC_000001.9:g.159451074G>A NCBI36
NG_013352.1:g.20346G>A
NG_029043.1:g.4364G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4719G>A
ENST00000678492.1:n.4483G>A
Search 100 bp 5'
Search 100 bp 3'