Canonical Allele Identifier: CA931721889

Gene: ABCC2

Linked Data

• gnomAD v3: 10-99844667-T-TGTC
• gnomAD v4: 10-99844667-T-TGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844669_99844671dup , CM000672.2:g.99844669_99844671dup	GRCh38
NC_000010.10:g.101604426_101604428dup , CM000672.1:g.101604426_101604428dup	GRCh37
NC_000010.9:g.101594416_101594418dup	NCBI36
NG_011798.1:g.66964_66966dup
NG_011798.2:g.67072_67074dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+204_3987+206dup MANE Select	ENSP00000497274.1:n.3987+204_3987+206dup
ENST00000649459.1:n.335+204_335+206dup
ENST00000370449.8:c.3987+204_3987+206dup	ENSP00000359478.4:n.3987+204_3987+206dup
NM_000392.4:c.3987+204_3987+206dup	NP_000383.1:n.3987+204_3987+206dup
XM_006717630.2:c.3291+204_3291+206dup	XP_006717693.1:n.3291+204_3291+206dup
XR_945604.1:n.4176+204_4176+206dup
XR_945605.1:n.4051+204_4051+206dup
NM_000392.5:c.3987+204_3987+206dup MANE Select	NP_000383.2:n.3987+204_3987+206dup
XM_006717630.3:c.3291+204_3291+206dup	XP_006717693.1:n.3291+204_3291+206dup
XR_945604.3:n.4230+204_4230+206dup
XR_945605.3:n.4103+204_4103+206dup