Canonical Allele Identifier: CA1931489031

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830313A= , CM000672.2:g.99830313A=	GRCh38
NC_000010.10:g.101590070A= , CM000672.1:g.101590070A=	GRCh37
NC_000010.9:g.101580060A=	NCBI36
NG_011798.1:g.52608A=
NG_011798.2:g.52716A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2627A= MANE Select	ENSP00000497274.1:p.Asp876=
ENST00000370449.8:c.2627A=	ENSP00000359478.4:p.Asp876=
NM_000392.4:c.2627A=	NP_000383.1:p.Asp876=
XM_006717630.2:c.1931A=	XP_006717693.1:p.Asp644=
XM_006717631.2:c.*54A=	XP_006717694.1:n.*54A=
XM_011539291.1:c.2627A=	XP_011537593.1:p.Asp876=
XR_945604.1:n.2816A=
XR_945605.1:n.2818A=
NM_000392.5:c.2627A= MANE Select	NP_000383.2:p.Asp876=
XM_006717630.3:c.1931A=	XP_006717693.1:p.Asp644=
XM_006717631.4:c.*54A=	XP_006717694.1:n.*54A=
XM_011539291.3:c.2627A=	XP_011537593.1:p.Asp876=
XR_945604.3:n.2870A=
XR_945605.3:n.2870A=