Canonical Allele Identifier: CA1931496001

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836056G= , CM000672.2:g.99836056G=	GRCh38
NC_000010.10:g.101595813G= , CM000672.1:g.101595813G=	GRCh37
NC_000010.9:g.101585803G=	NCBI36
NG_011798.1:g.58351G=
NG_011798.2:g.58459G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3415-35G= MANE Select	ENSP00000497274.1:n.3415-35G=
ENST00000370449.8:c.3415-35G=	ENSP00000359478.4:n.3415-35G=
NM_000392.4:c.3415-35G=	NP_000383.1:n.3415-35G=
XM_006717630.2:c.2719-35G=	XP_006717693.1:n.2719-35G=
XR_945604.1:n.3604-35G=
XR_945605.1:n.3606-35G=
NM_000392.5:c.3415-35G= MANE Select	NP_000383.2:n.3415-35G=
XM_006717630.3:c.2719-35G=	XP_006717693.1:n.2719-35G=
XR_945604.3:n.3658-35G=
XR_945605.3:n.3658-35G=