Canonical Allele Identifier: CA1931511698

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844182T= , CM000672.2:g.99844182T=	GRCh38
NC_000010.10:g.101603939T= , CM000672.1:g.101603939T=	GRCh37
NC_000010.9:g.101593929T=	NCBI36
NG_011798.1:g.66477T=
NG_011798.2:g.66585T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-140T= MANE Select	ENSP00000497274.1:n.3844-140T=
ENST00000649459.1:n.192-140T=
ENST00000370449.8:c.3844-140T=	ENSP00000359478.4:n.3844-140T=
NM_000392.4:c.3844-140T=	NP_000383.1:n.3844-140T=
XM_006717630.2:c.3148-140T=	XP_006717693.1:n.3148-140T=
XR_945604.1:n.4033-140T=
XR_945605.1:n.3908-140T=
NM_000392.5:c.3844-140T= MANE Select	NP_000383.2:n.3844-140T=
XM_006717630.3:c.3148-140T=	XP_006717693.1:n.3148-140T=
XR_945604.3:n.4087-140T=
XR_945605.3:n.3960-140T=