Canonical Allele Identifier: CA2610497791

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99844592-C-CAGGGCAGAGGAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844592_99844593insAGGGCAGAGGAAG , CM000672.2:g.99844592_99844593insAGGGCAGAGGAAG	GRCh38
NC_000010.10:g.101604349_101604350insAGGGCAGAGGAAG , CM000672.1:g.101604349_101604350insAGGGCAGAGGAAG	GRCh37
NC_000010.9:g.101594339_101594340insAGGGCAGAGGAAG	NCBI36
NG_011798.1:g.66887_66888insAGGGCAGAGGAAG
NG_011798.2:g.66995_66996insAGGGCAGAGGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+127_3987+128insAGGGCAGAGGAAG MANE Select	ENSP00000497274.1:n.3987+127_3987+128insAGGGCAGAGGAAG
ENST00000649459.1:n.335+127_335+128insAGGGCAGAGGAAG
ENST00000370449.8:c.3987+127_3987+128insAGGGCAGAGGAAG	ENSP00000359478.4:n.3987+127_3987+128insAGGGCAGAGGAAG
NM_000392.4:c.3987+127_3987+128insAGGGCAGAGGAAG	NP_000383.1:n.3987+127_3987+128insAGGGCAGAGGAAG
XM_006717630.2:c.3291+127_3291+128insAGGGCAGAGGAAG	XP_006717693.1:n.3291+127_3291+128insAGGGCAGAGGAAG
XR_945604.1:n.4176+127_4176+128insAGGGCAGAGGAAG
XR_945605.1:n.4051+127_4051+128insAGGGCAGAGGAAG
NM_000392.5:c.3987+127_3987+128insAGGGCAGAGGAAG MANE Select	NP_000383.2:n.3987+127_3987+128insAGGGCAGAGGAAG
XM_006717630.3:c.3291+127_3291+128insAGGGCAGAGGAAG	XP_006717693.1:n.3291+127_3291+128insAGGGCAGAGGAAG
XR_945604.3:n.4230+127_4230+128insAGGGCAGAGGAAG
XR_945605.3:n.4103+127_4103+128insAGGGCAGAGGAAG