Canonical Allele Identifier: CA1008396608
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665965309
gnomAD v3: 1-161214693-T-C
gnomAD v4: 1-161214693-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214693T>C , CM000663.2:g.161214693T>C GRCh38
NC_000001.10:g.161184483T>C , CM000663.1:g.161184483T>C GRCh37
NC_000001.9:g.159451107T>C NCBI36
NG_013352.1:g.20379T>C
NG_029043.1:g.4397T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4752T>C
ENST00000678492.1:n.4516T>C
Search 100 bp 5'
Search 100 bp 3'