Canonical Allele Identifier: CA1931511677

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844145T= , CM000672.2:g.99844145T=	GRCh38
NC_000010.10:g.101603902T= , CM000672.1:g.101603902T=	GRCh37
NC_000010.9:g.101593892T=	NCBI36
NG_011798.1:g.66440T=
NG_011798.2:g.66548T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-177T= MANE Select	ENSP00000497274.1:n.3844-177T=
ENST00000649459.1:n.192-177T=
ENST00000370449.8:c.3844-177T=	ENSP00000359478.4:n.3844-177T=
NM_000392.4:c.3844-177T=	NP_000383.1:n.3844-177T=
XM_006717630.2:c.3148-177T=	XP_006717693.1:n.3148-177T=
XR_945604.1:n.4033-177T=
XR_945605.1:n.3908-177T=
NM_000392.5:c.3844-177T= MANE Select	NP_000383.2:n.3844-177T=
XM_006717630.3:c.3148-177T=	XP_006717693.1:n.3148-177T=
XR_945604.3:n.4087-177T=
XR_945605.3:n.3960-177T=