Canonical Allele Identifier: CA7953791
Gene: UQCRC2 HGNC NCBI
PDZD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 380582
dbSNP Id: rs4850

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21965441G>A , CM000678.2:g.21965441G>A GRCh38
NC_000016.9:g.21976762G>A , CM000678.1:g.21976762G>A GRCh37
NC_000016.8:g.21884263G>A NCBI36
NG_042228.1:g.17378G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000268379.9:c.548G>A (UQCRC2) MANE Select ENSP00000268379.4:p.Arg183Gln
ENST00000268379.8:c.548G>A (UQCRC2) ENSP00000268379.4:p.Arg183Gln
ENST00000561553.5:c.548G>A (UQCRC2) ENSP00000456232.1:p.Arg183Gln
ENST00000563711.5:n.728G>A (UQCRC2)
ENST00000563898.5:c.548G>A (UQCRC2) ENSP00000456738.1:p.Arg183Gln
ENST00000565331.5:c.464G>A (UQCRC2) ENSP00000455088.1:p.Arg155Gln
ENST00000567597.1:n.220G>A (UQCRC2)
NM_003366.2:c.548G>A (UQCRC2) NP_003357.2:p.Arg183Gln
NM_003366.3:c.548G>A (UQCRC2) NP_003357.2:p.Arg183Gln
XM_011545785.1:c.787-7824C>T (PDZD9) XP_011544087.1:n.787-7824C>T
XM_011545785.3:c.787-7824C>T (PDZD9) XP_011544087.1:n.787-7824C>T
XM_017023109.1:c.607-7824C>T (PDZD9) XP_016878598.1:n.607-7824C>T
XM_017023110.1:c.601-7824C>T (PDZD9) XP_016878599.1:n.601-7824C>T
NM_003366.4:c.548G>A (UQCRC2) MANE Select NP_003357.2:p.Arg183Gln