Canonical Allele Identifier: CA2610496419

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99830605-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830607del , CM000672.2:g.99830607del	GRCh38
NC_000010.10:g.101590364del , CM000672.1:g.101590364del	GRCh37
NC_000010.9:g.101580354del	NCBI36
NG_011798.1:g.52902del
NG_011798.2:g.53010del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-109del MANE Select	ENSP00000497274.1:n.2748-109del
ENST00000370449.8:c.2748-109del	ENSP00000359478.4:n.2748-109del
NM_000392.4:c.2748-109del	NP_000383.1:n.2748-109del
XM_006717630.2:c.2052-109del	XP_006717693.1:n.2052-109del
XM_011539291.1:c.2747+174del	XP_011537593.1:n.2747+174del
XR_945604.1:n.2937-109del
XR_945605.1:n.2939-109del
NM_000392.5:c.2748-109del MANE Select	NP_000383.2:n.2748-109del
XM_006717630.3:c.2052-109del	XP_006717693.1:n.2052-109del
XM_011539291.3:c.2747+174del	XP_011537593.1:n.2747+174del
XR_945604.3:n.2991-109del
XR_945605.3:n.2991-109del