Canonical Allele Identifier: CA1931489589

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830584C= , CM000672.2:g.99830584C=	GRCh38
NC_000010.10:g.101590341C= , CM000672.1:g.101590341C=	GRCh37
NC_000010.9:g.101580331C=	NCBI36
NG_011798.1:g.52879C=
NG_011798.2:g.52987C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-132C= MANE Select	ENSP00000497274.1:n.2748-132C=
ENST00000370449.8:c.2748-132C=	ENSP00000359478.4:n.2748-132C=
NM_000392.4:c.2748-132C=	NP_000383.1:n.2748-132C=
XM_006717630.2:c.2052-132C=	XP_006717693.1:n.2052-132C=
XM_011539291.1:c.2747+151C=	XP_011537593.1:n.2747+151C=
XR_945604.1:n.2937-132C=
XR_945605.1:n.2939-132C=
NM_000392.5:c.2748-132C= MANE Select	NP_000383.2:n.2748-132C=
XM_006717630.3:c.2052-132C=	XP_006717693.1:n.2052-132C=
XM_011539291.3:c.2747+151C=	XP_011537593.1:n.2747+151C=
XR_945604.3:n.2991-132C=
XR_945605.3:n.2991-132C=