Canonical Allele Identifier: CA1931512146

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844478A= , CM000672.2:g.99844478A=	GRCh38
NC_000010.10:g.101604235A= , CM000672.1:g.101604235A=	GRCh37
NC_000010.9:g.101594225A=	NCBI36
NG_011798.1:g.66773A=
NG_011798.2:g.66881A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+13A= MANE Select	ENSP00000497274.1:n.3987+13A=
ENST00000649459.1:n.335+13A=
ENST00000370449.8:c.3987+13A=	ENSP00000359478.4:n.3987+13A=
NM_000392.4:c.3987+13A=	NP_000383.1:n.3987+13A=
XM_006717630.2:c.3291+13A=	XP_006717693.1:n.3291+13A=
XR_945604.1:n.4176+13A=
XR_945605.1:n.4051+13A=
NM_000392.5:c.3987+13A= MANE Select	NP_000383.2:n.3987+13A=
XM_006717630.3:c.3291+13A=	XP_006717693.1:n.3291+13A=
XR_945604.3:n.4230+13A=
XR_945605.3:n.4103+13A=