Canonical Allele Identifier: CA1931492145

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99811621A= , CM000672.2:g.99811621A=	GRCh38
NC_000010.10:g.101571378A= , CM000672.1:g.101571378A=	GRCh37
NC_000010.9:g.101561368A=	NCBI36
NG_011798.1:g.33916A=
NG_011798.2:g.34024A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.1967+19A= MANE Select	ENSP00000497274.1:n.1967+19A=
ENST00000370449.8:c.1967+19A=	ENSP00000359478.4:n.1967+19A=
NM_000392.4:c.1967+19A=	NP_000383.1:n.1967+19A=
XM_006717630.2:c.1271+19A=	XP_006717693.1:n.1271+19A=
XM_006717631.2:c.1967+19A=	XP_006717694.1:n.1967+19A=
XM_011539291.1:c.1967+19A=	XP_011537593.1:n.1967+19A=
XR_945604.1:n.2156+19A=
XR_945605.1:n.2158+19A=
NM_000392.5:c.1967+19A= MANE Select	NP_000383.2:n.1967+19A=
XM_006717630.3:c.1271+19A=	XP_006717693.1:n.1271+19A=
XM_006717631.4:c.1967+19A=	XP_006717694.1:n.1967+19A=
XM_011539291.3:c.1967+19A=	XP_011537593.1:n.1967+19A=
XM_017015675.2:c.1967+19A=	XP_016871164.1:n.1967+19A=
XR_945604.3:n.2210+19A=
XR_945605.3:n.2210+19A=