Canonical Allele Identifier: CA1931495993

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836047C= , CM000672.2:g.99836047C=	GRCh38
NC_000010.10:g.101595804C= , CM000672.1:g.101595804C=	GRCh37
NC_000010.9:g.101585794C=	NCBI36
NG_011798.1:g.58342C=
NG_011798.2:g.58450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-44C= MANE Select	ENSP00000497274.1:n.3415-44C=
ENST00000370449.8:c.3415-44C=	ENSP00000359478.4:n.3415-44C=
NM_000392.4:c.3415-44C=	NP_000383.1:n.3415-44C=
XM_006717630.2:c.2719-44C=	XP_006717693.1:n.2719-44C=
XR_945604.1:n.3604-44C=
XR_945605.1:n.3606-44C=
NM_000392.5:c.3415-44C= MANE Select	NP_000383.2:n.3415-44C=
XM_006717630.3:c.2719-44C=	XP_006717693.1:n.2719-44C=
XR_945604.3:n.3658-44C=
XR_945605.3:n.3658-44C=