Canonical Allele Identifier: CA2610497309

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99836398-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836406_99836407dup , CM000672.2:g.99836406_99836407dup	GRCh38
NC_000010.10:g.101596163_101596164dup , CM000672.1:g.101596163_101596164dup	GRCh37
NC_000010.9:g.101586153_101586154dup	NCBI36
NG_011798.1:g.58701_58702dup
NG_011798.2:g.58809_58810dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3614+116_3614+117dup MANE Select	ENSP00000497274.1:n.3614+116_3614+117dup
ENST00000370449.8:c.3614+116_3614+117dup	ENSP00000359478.4:n.3614+116_3614+117dup
NM_000392.4:c.3614+116_3614+117dup	NP_000383.1:n.3614+116_3614+117dup
XM_006717630.2:c.2918+116_2918+117dup	XP_006717693.1:n.2918+116_2918+117dup
XR_945604.1:n.3803+116_3803+117dup
XR_945605.1:n.3805+116_3805+117dup
NM_000392.5:c.3614+116_3614+117dup MANE Select	NP_000383.2:n.3614+116_3614+117dup
XM_006717630.3:c.2918+116_2918+117dup	XP_006717693.1:n.2918+116_2918+117dup
XR_945604.3:n.3857+116_3857+117dup
XR_945605.3:n.3857+116_3857+117dup