Canonical Allele Identifier: CA2530861622

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845841-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845844_99845845del , CM000672.2:g.99845844_99845845del	GRCh38
NC_000010.10:g.101605601_101605602del , CM000672.1:g.101605601_101605602del	GRCh37
NC_000010.9:g.101595591_101595592del	NCBI36
NG_011798.1:g.68139_68140del
NG_011798.2:g.68247_68248del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4146+62_4146+63del MANE Select	ENSP00000497274.1:n.4146+62_4146+63del
ENST00000648523.1:c.34+62_34+63del
ENST00000649459.1:n.494+62_494+63del
ENST00000370449.8:c.4146+62_4146+63del	ENSP00000359478.4:n.4146+62_4146+63del
NM_000392.4:c.4146+62_4146+63del	NP_000383.1:n.4146+62_4146+63del
XM_006717630.2:c.3450+62_3450+63del	XP_006717693.1:n.3450+62_3450+63del
XR_945604.1:n.4276+62_4276+63del
XR_945605.1:n.4210+62_4210+63del
NM_000392.5:c.4146+62_4146+63del MANE Select	NP_000383.2:n.4146+62_4146+63del
XM_006717630.3:c.3450+62_3450+63del	XP_006717693.1:n.3450+62_3450+63del
XR_945604.3:n.4330+62_4330+63del
XR_945605.3:n.4262+62_4262+63del