Canonical Allele Identifier: CA1931512439

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844671G= , CM000672.2:g.99844671G=	GRCh38
NC_000010.10:g.101604428G= , CM000672.1:g.101604428G=	GRCh37
NC_000010.9:g.101594418G=	NCBI36
NG_011798.1:g.66966G=
NG_011798.2:g.67074G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+206G= MANE Select	ENSP00000497274.1:n.3987+206G=
ENST00000649459.1:n.335+206G=
ENST00000370449.8:c.3987+206G=	ENSP00000359478.4:n.3987+206G=
NM_000392.4:c.3987+206G=	NP_000383.1:n.3987+206G=
XM_006717630.2:c.3291+206G=	XP_006717693.1:n.3291+206G=
XR_945604.1:n.4176+206G=
XR_945605.1:n.4051+206G=
NM_000392.5:c.3987+206G= MANE Select	NP_000383.2:n.3987+206G=
XM_006717630.3:c.3291+206G=	XP_006717693.1:n.3291+206G=
XR_945604.3:n.4230+206G=
XR_945605.3:n.4103+206G=