Canonical Allele Identifier: CA2610496393

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99830574-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830574G>A , CM000672.2:g.99830574G>A	GRCh38
NC_000010.10:g.101590331G>A , CM000672.1:g.101590331G>A	GRCh37
NC_000010.9:g.101580321G>A	NCBI36
NG_011798.1:g.52869G>A
NG_011798.2:g.52977G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-142G>A MANE Select	ENSP00000497274.1:n.2748-142G>A
ENST00000370449.8:c.2748-142G>A	ENSP00000359478.4:n.2748-142G>A
NM_000392.4:c.2748-142G>A	NP_000383.1:n.2748-142G>A
XM_006717630.2:c.2052-142G>A	XP_006717693.1:n.2052-142G>A
XM_011539291.1:c.2747+141G>A	XP_011537593.1:n.2747+141G>A
XR_945604.1:n.2937-142G>A
XR_945605.1:n.2939-142G>A
NM_000392.5:c.2748-142G>A MANE Select	NP_000383.2:n.2748-142G>A
XM_006717630.3:c.2052-142G>A	XP_006717693.1:n.2052-142G>A
XM_011539291.3:c.2747+141G>A	XP_011537593.1:n.2747+141G>A
XR_945604.3:n.2991-142G>A
XR_945605.3:n.2991-142G>A