Canonical Allele Identifier: CA2574638599
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836071del , CM000672.2:g.99836071del GRCh38
NC_000010.10:g.101595828del , CM000672.1:g.101595828del GRCh37
NC_000010.9:g.101585818del NCBI36
NG_011798.1:g.58366del
NG_011798.2:g.58474del

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3415-20del MANE Select ENSP00000497274.1:n.3415-20del
ENST00000370449.8:c.3415-20del ENSP00000359478.4:n.3415-20del
NM_000392.4:c.3415-20del NP_000383.1:n.3415-20del
XM_006717630.2:c.2719-20del XP_006717693.1:n.2719-20del
XR_945604.1:n.3604-20del
XR_945605.1:n.3606-20del
NM_000392.5:c.3415-20del MANE Select NP_000383.2:n.3415-20del
XM_006717630.3:c.2719-20del XP_006717693.1:n.2719-20del
XR_945604.3:n.3658-20del
XR_945605.3:n.3658-20del