Canonical Allele Identifier: CA2789199232
Gene: ABCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99851362del , CM000672.2:g.99851362del GRCh38
NC_000010.10:g.101611119del , CM000672.1:g.101611119del GRCh37
NC_000010.9:g.101601109del NCBI36
NG_011798.1:g.73657del
NG_011798.2:g.73765del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.4509-140del MANE Select ENSP00000497274.1:n.4509-140del
ENST00000648523.1:c.579-140del
ENST00000370449.8:c.4509-140del ENSP00000359478.4:n.4509-140del
NM_000392.4:c.4509-140del NP_000383.1:n.4509-140del
XM_006717630.2:c.3813-140del XP_006717693.1:n.3813-140del
XR_945605.1:n.4573-140del
NM_000392.5:c.4509-140del MANE Select NP_000383.2:n.4509-140del
XM_006717630.3:c.3813-140del XP_006717693.1:n.3813-140del
XR_945605.3:n.4625-140del
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