Canonical Allele Identifier: CA2632236253

Gene: UQCRC2 PDZD9

Linked Data

• gnomAD v4: 16-21974096-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21974096T>G , CM000678.2:g.21974096T>G	GRCh38
NC_000016.9:g.21985417T>G , CM000678.1:g.21985417T>G	GRCh37
NC_000016.8:g.21892918T>G	NCBI36
NG_042228.1:g.26033T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000268379.9:c.1047+120T>G (UQCRC2) MANE Select	ENSP00000268379.4:n.1047+120T>G
ENST00000268379.8:c.1047+120T>G (UQCRC2)	ENSP00000268379.4:n.1047+120T>G
ENST00000561553.5:c.1047+120T>G (UQCRC2)	ENSP00000456232.1:n.1047+120T>G
ENST00000563711.5:n.1227+120T>G (UQCRC2)
ENST00000563898.5:c.966+1974T>G (UQCRC2)	ENSP00000456738.1:n.966+1974T>G
NM_003366.2:c.1047+120T>G (UQCRC2)	NP_003357.2:n.1047+120T>G
NM_003366.3:c.1047+120T>G (UQCRC2)	NP_003357.2:n.1047+120T>G
XM_011545785.1:c.786+10180A>C (PDZD9)	XP_011544087.1:n.786+10180A>C
XM_011545785.3:c.786+10180A>C (PDZD9)	XP_011544087.1:n.786+10180A>C
XM_017023109.1:c.606+10180A>C (PDZD9)	XP_016878598.1:n.606+10180A>C
XM_017023110.1:c.600+10180A>C (PDZD9)	XP_016878599.1:n.600+10180A>C
NM_003366.4:c.1047+120T>G (UQCRC2) MANE Select	NP_003357.2:n.1047+120T>G