Canonical Allele Identifier: CA2610495337

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99818719-CCCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818724_99818727del , CM000672.2:g.99818724_99818727del	GRCh38
NC_000010.10:g.101578481_101578484del , CM000672.1:g.101578481_101578484del	GRCh37
NC_000010.9:g.101568471_101568474del	NCBI36
NG_011798.1:g.41019_41022del
NG_011798.2:g.41127_41130del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2272-66_2272-63del MANE Select	ENSP00000497274.1:n.2272-66_2272-63del
ENST00000370449.8:c.2272-66_2272-63del	ENSP00000359478.4:n.2272-66_2272-63del
NM_000392.4:c.2272-66_2272-63del	NP_000383.1:n.2272-66_2272-63del
XM_006717630.2:c.1576-66_1576-63del	XP_006717693.1:n.1576-66_1576-63del
XM_006717631.2:c.2272-66_2272-63del	XP_006717694.1:n.2272-66_2272-63del
XM_011539291.1:c.2272-66_2272-63del	XP_011537593.1:n.2272-66_2272-63del
XR_945604.1:n.2461-66_2461-63del
XR_945605.1:n.2463-66_2463-63del
NM_000392.5:c.2272-66_2272-63del MANE Select	NP_000383.2:n.2272-66_2272-63del
XM_006717630.3:c.1576-66_1576-63del	XP_006717693.1:n.1576-66_1576-63del
XM_006717631.4:c.2272-66_2272-63del	XP_006717694.1:n.2272-66_2272-63del
XM_011539291.3:c.2272-66_2272-63del	XP_011537593.1:n.2272-66_2272-63del
XM_017015675.2:c.2272-66_2272-63del	XP_016871164.1:n.2272-66_2272-63del
XR_945604.3:n.2515-66_2515-63del
XR_945605.3:n.2515-66_2515-63del