Canonical Allele Identifier: CA1931444669

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99782742G= , CM000672.2:g.99782742G=	GRCh38
NC_000010.10:g.101542499G= , CM000672.1:g.101542499G=	GRCh37
NC_000010.9:g.101532489G=	NCBI36
NG_011798.1:g.5037G=
NG_011798.2:g.5145G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.-103G= MANE Select	ENSP00000497274.1:n.-103G=
ENST00000647836.1:n.103G=
ENST00000648324.1:c.-103G=	ENSP00000497248.1:n.-103G=
ENST00000648689.1:c.-103G=	ENSP00000496972.1:n.-103G=
ENST00000649932.1:c.-103G=	ENSP00000498120.1:n.-103G=
ENST00000370449.8:c.-103G=	ENSP00000359478.4:n.-103G=
NM_000392.4:c.-103G=	NP_000383.1:n.-103G=
XM_006717631.2:c.-103G=	XP_006717694.1:n.-103G=
XM_011539291.1:c.-103G=	XP_011537593.1:n.-103G=
XR_945604.1:n.87G=
XR_945605.1:n.89G=
NM_000392.5:c.-103G= MANE Select	NP_000383.2:n.-103G=
XM_006717631.4:c.-103G=	XP_006717694.1:n.-103G=
XM_011539291.3:c.-103G=	XP_011537593.1:n.-103G=
XM_017015675.2:c.-103G=	XP_016871164.1:n.-103G=
XR_945604.3:n.141G=
XR_945605.3:n.141G=