Canonical Allele Identifier: CA1931484404

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851367A= , CM000672.2:g.99851367A=	GRCh38
NC_000010.10:g.101611124A= , CM000672.1:g.101611124A=	GRCh37
NC_000010.9:g.101601114A=	NCBI36
NG_011798.1:g.73662A=
NG_011798.2:g.73770A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4509-135A= MANE Select	ENSP00000497274.1:n.4509-135A=
ENST00000648523.1:c.579-135A=
ENST00000370449.8:c.4509-135A=	ENSP00000359478.4:n.4509-135A=
NM_000392.4:c.4509-135A=	NP_000383.1:n.4509-135A=
XM_006717630.2:c.3813-135A=	XP_006717693.1:n.3813-135A=
XR_945605.1:n.4573-135A=
NM_000392.5:c.4509-135A= MANE Select	NP_000383.2:n.4509-135A=
XM_006717630.3:c.3813-135A=	XP_006717693.1:n.3813-135A=
XR_945605.3:n.4625-135A=