Canonical Allele Identifier: CA1931489136

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830363G= , CM000672.2:g.99830363G=	GRCh38
NC_000010.10:g.101590120G= , CM000672.1:g.101590120G=	GRCh37
NC_000010.9:g.101580110G=	NCBI36
NG_011798.1:g.52658G=
NG_011798.2:g.52766G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000392.5:c.2677G= MANE Select	NP_000383.2:p.Glu893=
ENST00000647814.1:c.2677G= MANE Select	ENSP00000497274.1:p.Glu893=
NM_000392.4:c.2677G=	NP_000383.1:p.Glu893=
ENST00000370449.8:c.2677G=	ENSP00000359478.4:p.Glu893=
XM_006717630.2:c.1981G=	XP_006717693.1:p.Glu661=
XM_006717630.3:c.1981G=	XP_006717693.1:p.Glu661=
XM_006717631.2:c.*104G=	XP_006717694.1:n.*104G=
XM_006717631.4:c.*104G=	XP_006717694.1:n.*104G=
XM_011539291.1:c.2677G=	XP_011537593.1:p.Glu893=
XM_011539291.3:c.2677G=	XP_011537593.1:p.Glu893=
XR_945604.1:n.2866G=
XR_945604.3:n.2920G=
XR_945605.1:n.2868G=
XR_945605.3:n.2920G=