Canonical Allele Identifier: CA931735427

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038718848

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830435_99830436insC , CM000672.2:g.99830435_99830436insC	GRCh38
NC_000010.10:g.101590192_101590193insC , CM000672.1:g.101590192_101590193insC	GRCh37
NC_000010.9:g.101580182_101580183insC	NCBI36
NG_011798.1:g.52730_52731insC
NG_011798.2:g.52838_52839insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+2_2747+3insC MANE Select	ENSP00000497274.1:n.2747+2_2747+3insC
ENST00000370449.8:c.2747+2_2747+3insC	ENSP00000359478.4:n.2747+2_2747+3insC
NM_000392.4:c.2747+2_2747+3insC	NP_000383.1:n.2747+2_2747+3insC
XM_006717630.2:c.2051+2_2051+3insC	XP_006717693.1:n.2051+2_2051+3insC
XM_011539291.1:c.2747+2_2747+3insC	XP_011537593.1:n.2747+2_2747+3insC
XR_945604.1:n.2936+2_2936+3insC
XR_945605.1:n.2938+2_2938+3insC
NM_000392.5:c.2747+2_2747+3insC MANE Select	NP_000383.2:n.2747+2_2747+3insC
XM_006717630.3:c.2051+2_2051+3insC	XP_006717693.1:n.2051+2_2051+3insC
XM_011539291.3:c.2747+2_2747+3insC	XP_011537593.1:n.2747+2_2747+3insC
XR_945604.3:n.2990+2_2990+3insC
XR_945605.3:n.2990+2_2990+3insC