Canonical Allele Identifier: CA1931509303

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817351G= , CM000672.2:g.99817351G=	GRCh38
NC_000010.10:g.101577108G= , CM000672.1:g.101577108G=	GRCh37
NC_000010.9:g.101567098G=	NCBI36
NG_011798.1:g.39646G=
NG_011798.2:g.39754G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2138G= MANE Select	ENSP00000497274.1:p.Gly713=
ENST00000370449.8:c.2138G=	ENSP00000359478.4:p.Gly713=
NM_000392.4:c.2138G=	NP_000383.1:p.Gly713=
XM_006717630.2:c.1442G=	XP_006717693.1:p.Gly481=
XM_006717631.2:c.2138G=	XP_006717694.1:p.Gly713=
XM_011539291.1:c.2138G=	XP_011537593.1:p.Gly713=
XR_945604.1:n.2327G=
XR_945605.1:n.2329G=
NM_000392.5:c.2138G= MANE Select	NP_000383.2:p.Gly713=
XM_006717630.3:c.1442G=	XP_006717693.1:p.Gly481=
XM_006717631.4:c.2138G=	XP_006717694.1:p.Gly713=
XM_011539291.3:c.2138G=	XP_011537593.1:p.Gly713=
XM_017015675.2:c.2138G=	XP_016871164.1:p.Gly713=
XR_945604.3:n.2381G=
XR_945605.3:n.2381G=