Canonical Allele Identifier: CA1931489485

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830522G= , CM000672.2:g.99830522G=	GRCh38
NC_000010.10:g.101590279G= , CM000672.1:g.101590279G=	GRCh37
NC_000010.9:g.101580269G=	NCBI36
NG_011798.1:g.52817G=
NG_011798.2:g.52925G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+89G= MANE Select	ENSP00000497274.1:n.2747+89G=
ENST00000370449.8:c.2747+89G=	ENSP00000359478.4:n.2747+89G=
NM_000392.4:c.2747+89G=	NP_000383.1:n.2747+89G=
XM_006717630.2:c.2051+89G=	XP_006717693.1:n.2051+89G=
XM_011539291.1:c.2747+89G=	XP_011537593.1:n.2747+89G=
XR_945604.1:n.2936+89G=
XR_945605.1:n.2938+89G=
NM_000392.5:c.2747+89G= MANE Select	NP_000383.2:n.2747+89G=
XM_006717630.3:c.2051+89G=	XP_006717693.1:n.2051+89G=
XM_011539291.3:c.2747+89G=	XP_011537593.1:n.2747+89G=
XR_945604.3:n.2990+89G=
XR_945605.3:n.2990+89G=