Canonical Allele Identifier: CA1931458907

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99799313C= , CM000672.2:g.99799313C=	GRCh38
NC_000010.10:g.101559070C= , CM000672.1:g.101559070C=	GRCh37
NC_000010.9:g.101549060C=	NCBI36
NG_011798.1:g.21608C=
NG_011798.2:g.21716C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000392.5:c.974C= MANE Select	NP_000383.2:p.Ser325=
ENST00000647814.1:c.974C= MANE Select	ENSP00000497274.1:p.Ser325=
NM_000392.4:c.974C=	NP_000383.1:p.Ser325=
ENST00000370449.8:c.974C=	ENSP00000359478.4:p.Ser325=
XM_006717630.2:c.278C=	XP_006717693.1:p.Ser93=
XM_006717630.3:c.278C=	XP_006717693.1:p.Ser93=
XM_006717631.2:c.974C=	XP_006717694.1:p.Ser325=
XM_006717631.4:c.974C=	XP_006717694.1:p.Ser325=
XM_011539291.1:c.974C=	XP_011537593.1:p.Ser325=
XM_011539291.3:c.974C=	XP_011537593.1:p.Ser325=
XM_017015675.2:c.974C=	XP_016871164.1:p.Ser325=
XR_945604.1:n.1163C=
XR_945604.3:n.1217C=
XR_945605.1:n.1165C=
XR_945605.3:n.1217C=