Canonical Allele Identifier: CA1931489173

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830379C= , CM000672.2:g.99830379C=	GRCh38
NC_000010.10:g.101590136C= , CM000672.1:g.101590136C=	GRCh37
NC_000010.9:g.101580126C=	NCBI36
NG_011798.1:g.52674C=
NG_011798.2:g.52782C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2693C= MANE Select	ENSP00000497274.1:p.Ala898=
ENST00000370449.8:c.2693C=	ENSP00000359478.4:p.Ala898=
NM_000392.4:c.2693C=	NP_000383.1:p.Ala898=
XM_006717630.2:c.1997C=	XP_006717693.1:p.Ala666=
XM_006717631.2:c.*120C=	XP_006717694.1:n.*120C=
XM_011539291.1:c.2693C=	XP_011537593.1:p.Ala898=
XR_945604.1:n.2882C=
XR_945605.1:n.2884C=
NM_000392.5:c.2693C= MANE Select	NP_000383.2:p.Ala898=
XM_006717630.3:c.1997C=	XP_006717693.1:p.Ala666=
XM_006717631.4:c.*120C=	XP_006717694.1:n.*120C=
XM_011539291.3:c.2693C=	XP_011537593.1:p.Ala898=
XR_945604.3:n.2936C=
XR_945605.3:n.2936C=