Canonical Allele Identifier: CA2610497282
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836339_99836340insCCAAATAC , CM000672.2:g.99836339_99836340insCCAAATAC GRCh38
NC_000010.10:g.101596096_101596097insCCAAATAC , CM000672.1:g.101596096_101596097insCCAAATAC GRCh37
NC_000010.9:g.101586086_101586087insCCAAATAC NCBI36
NG_011798.1:g.58634_58635insCCAAATAC
NG_011798.2:g.58742_58743insCCAAATAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3614+49_3614+50insCCAAATAC MANE Select ENSP00000497274.1:n.3614+49_3614+50insCCAAATAC
ENST00000370449.8:c.3614+49_3614+50insCCAAATAC ENSP00000359478.4:n.3614+49_3614+50insCCAAATAC
NM_000392.4:c.3614+49_3614+50insCCAAATAC NP_000383.1:n.3614+49_3614+50insCCAAATAC
XM_006717630.2:c.2918+49_2918+50insCCAAATAC XP_006717693.1:n.2918+49_2918+50insCCAAATAC
XR_945604.1:n.3803+49_3803+50insCCAAATAC
XR_945605.1:n.3805+49_3805+50insCCAAATAC
NM_000392.5:c.3614+49_3614+50insCCAAATAC MANE Select NP_000383.2:n.3614+49_3614+50insCCAAATAC
XM_006717630.3:c.2918+49_2918+50insCCAAATAC XP_006717693.1:n.2918+49_2918+50insCCAAATAC
XR_945604.3:n.3857+49_3857+50insCCAAATAC
XR_945605.3:n.3857+49_3857+50insCCAAATAC