Canonical Allele Identifier: CA1931489176

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830384T= , CM000672.2:g.99830384T=	GRCh38
NC_000010.10:g.101590141T= , CM000672.1:g.101590141T=	GRCh37
NC_000010.9:g.101580131T=	NCBI36
NG_011798.1:g.52679T=
NG_011798.2:g.52787T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2698T= MANE Select	ENSP00000497274.1:p.Ser900=
ENST00000370449.8:c.2698T=	ENSP00000359478.4:p.Ser900=
NM_000392.4:c.2698T=	NP_000383.1:p.Ser900=
XM_006717630.2:c.2002T=	XP_006717693.1:p.Ser668=
XM_006717631.2:c.*125T=	XP_006717694.1:n.*125T=
XM_011539291.1:c.2698T=	XP_011537593.1:p.Ser900=
XR_945604.1:n.2887T=
XR_945605.1:n.2889T=
NM_000392.5:c.2698T= MANE Select	NP_000383.2:p.Ser900=
XM_006717630.3:c.2002T=	XP_006717693.1:p.Ser668=
XM_006717631.4:c.*125T=	XP_006717694.1:n.*125T=
XM_011539291.3:c.2698T=	XP_011537593.1:p.Ser900=
XR_945604.3:n.2941T=
XR_945605.3:n.2941T=