Canonical Allele Identifier: CA1931511866

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844331G= , CM000672.2:g.99844331G=	GRCh38
NC_000010.10:g.101604088G= , CM000672.1:g.101604088G=	GRCh37
NC_000010.9:g.101594078G=	NCBI36
NG_011798.1:g.66626G=
NG_011798.2:g.66734G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3853G= MANE Select	ENSP00000497274.1:p.Val1285=
ENST00000649459.1:n.201G=
ENST00000370449.8:c.3853G=	ENSP00000359478.4:p.Val1285=
NM_000392.4:c.3853G=	NP_000383.1:p.Val1285=
XM_006717630.2:c.3157G=	XP_006717693.1:p.Val1053=
XR_945604.1:n.4042G=
XR_945605.1:n.3917G=
NM_000392.5:c.3853G= MANE Select	NP_000383.2:p.Val1285=
XM_006717630.3:c.3157G=	XP_006717693.1:p.Val1053=
XR_945604.3:n.4096G=
XR_945605.3:n.3969G=