Canonical Allele Identifier: CA1931489180

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830385C= , CM000672.2:g.99830385C=	GRCh38
NC_000010.10:g.101590142C= , CM000672.1:g.101590142C=	GRCh37
NC_000010.9:g.101580132C=	NCBI36
NG_011798.1:g.52680C=
NG_011798.2:g.52788C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2699C= MANE Select	ENSP00000497274.1:p.Ser900=
ENST00000370449.8:c.2699C=	ENSP00000359478.4:p.Ser900=
NM_000392.4:c.2699C=	NP_000383.1:p.Ser900=
XM_006717630.2:c.2003C=	XP_006717693.1:p.Ser668=
XM_006717631.2:c.*126C=	XP_006717694.1:n.*126C=
XM_011539291.1:c.2699C=	XP_011537593.1:p.Ser900=
XR_945604.1:n.2888C=
XR_945605.1:n.2890C=
NM_000392.5:c.2699C= MANE Select	NP_000383.2:p.Ser900=
XM_006717630.3:c.2003C=	XP_006717693.1:p.Ser668=
XM_006717631.4:c.*126C=	XP_006717694.1:n.*126C=
XM_011539291.3:c.2699C=	XP_011537593.1:p.Ser900=
XR_945604.3:n.2942C=
XR_945605.3:n.2942C=