Canonical Allele Identifier: CA1931509420

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817400G= , CM000672.2:g.99817400G=	GRCh38
NC_000010.10:g.101577157G= , CM000672.1:g.101577157G=	GRCh37
NC_000010.9:g.101567147G=	NCBI36
NG_011798.1:g.39695G=
NG_011798.2:g.39803G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2187G= MANE Select	ENSP00000497274.1:p.Arg729=
ENST00000370449.8:c.2187G=	ENSP00000359478.4:p.Arg729=
NM_000392.4:c.2187G=	NP_000383.1:p.Arg729=
XM_006717630.2:c.1491G=	XP_006717693.1:p.Arg497=
XM_006717631.2:c.2187G=	XP_006717694.1:p.Arg729=
XM_011539291.1:c.2187G=	XP_011537593.1:p.Arg729=
XR_945604.1:n.2376G=
XR_945605.1:n.2378G=
NM_000392.5:c.2187G= MANE Select	NP_000383.2:p.Arg729=
XM_006717630.3:c.1491G=	XP_006717693.1:p.Arg497=
XM_006717631.4:c.2187G=	XP_006717694.1:p.Arg729=
XM_011539291.3:c.2187G=	XP_011537593.1:p.Arg729=
XM_017015675.2:c.2187G=	XP_016871164.1:p.Arg729=
XR_945604.3:n.2430G=
XR_945605.3:n.2430G=