Canonical Allele Identifier: CA1931512449
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2038993422

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844673_99844674insATCACACAGACTTACCGCAGCTGA , CM000672.2:g.99844673_99844674insATCACACAGACTTACCGCAGCTGA GRCh38
NC_000010.10:g.101604430_101604431insATCACACAGACTTACCGCAGCTGA , CM000672.1:g.101604430_101604431insATCACACAGACTTACCGCAGCTGA GRCh37
NC_000010.9:g.101594420_101594421insATCACACAGACTTACCGCAGCTGA NCBI36
NG_011798.1:g.66968_66969insATCACACAGACTTACCGCAGCTGA
NG_011798.2:g.67076_67077insATCACACAGACTTACCGCAGCTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3987+208_3987+209insATCACACAGACTTACCGCAGCTGA MANE Select ENSP00000497274.1:n.3987+208_3987+209insATCACACAGACTTACCGCAGC...
ENST00000649459.1:n.335+208_335+209insATCACACAGACTTACCGCAGCTGA
ENST00000370449.8:c.3987+208_3987+209insATCACACAGACTTACCGCAGCTGA ENSP00000359478.4:n.3987+208_3987+209insATCACACAGACTTACCGCAGC...
NM_000392.4:c.3987+208_3987+209insATCACACAGACTTACCGCAGCTGA NP_000383.1:n.3987+208_3987+209insATCACACAGACTTACCGCAGCTGA
XM_006717630.2:c.3291+208_3291+209insATCACACAGACTTACCGCAGCTGA XP_006717693.1:n.3291+208_3291+209insATCACACAGACTTACCGCAGCTGA...
XR_945604.1:n.4176+208_4176+209insATCACACAGACTTACCGCAGCTGA
XR_945605.1:n.4051+208_4051+209insATCACACAGACTTACCGCAGCTGA
NM_000392.5:c.3987+208_3987+209insATCACACAGACTTACCGCAGCTGA MANE Select NP_000383.2:n.3987+208_3987+209insATCACACAGACTTACCGCAGCTGA
XM_006717630.3:c.3291+208_3291+209insATCACACAGACTTACCGCAGCTGA XP_006717693.1:n.3291+208_3291+209insATCACACAGACTTACCGCAGCTGA...
XR_945604.3:n.4230+208_4230+209insATCACACAGACTTACCGCAGCTGA
XR_945605.3:n.4103+208_4103+209insATCACACAGACTTACCGCAGCTGA