Canonical Allele Identifier: CA2610497264

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99836290-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836292_99836293del , CM000672.2:g.99836292_99836293del	GRCh38
NC_000010.10:g.101596049_101596050del , CM000672.1:g.101596049_101596050del	GRCh37
NC_000010.9:g.101586039_101586040del	NCBI36
NG_011798.1:g.58587_58588del
NG_011798.2:g.58695_58696del

Transcript Alleles

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