Canonical Allele Identifier: CA1931489664

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038722516

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830643_99830646del , CM000672.2:g.99830643_99830646del	GRCh38
NC_000010.10:g.101590400_101590403del , CM000672.1:g.101590400_101590403del	GRCh37
NC_000010.9:g.101580390_101580393del	NCBI36
NG_011798.1:g.52938_52941del
NG_011798.2:g.53046_53049del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-73_2748-70del MANE Select	ENSP00000497274.1:n.2748-73_2748-70del
ENST00000370449.8:c.2748-73_2748-70del	ENSP00000359478.4:n.2748-73_2748-70del
NM_000392.4:c.2748-73_2748-70del	NP_000383.1:n.2748-73_2748-70del
XM_006717630.2:c.2052-73_2052-70del	XP_006717693.1:n.2052-73_2052-70del
XM_011539291.1:c.2747+210_2747+213del	XP_011537593.1:n.2747+210_2747+213del
XR_945604.1:n.2937-73_2937-70del
XR_945605.1:n.2939-73_2939-70del
NM_000392.5:c.2748-73_2748-70del MANE Select	NP_000383.2:n.2748-73_2748-70del
XM_006717630.3:c.2052-73_2052-70del	XP_006717693.1:n.2052-73_2052-70del
XM_011539291.3:c.2747+210_2747+213del	XP_011537593.1:n.2747+210_2747+213del
XR_945604.3:n.2991-73_2991-70del
XR_945605.3:n.2991-73_2991-70del