Canonical Allele Identifier: CA212867205
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs879546361
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844406del , CM000672.2:g.99844406del GRCh38
NC_000010.10:g.101604163del , CM000672.1:g.101604163del GRCh37
NC_000010.9:g.101594153del NCBI36
NG_011798.1:g.66701del
NG_011798.2:g.66809del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3928del MANE Select ENSP00000497274.1:p.Arg1310AspfsTer?
ENST00000649459.1:n.276del
ENST00000370449.8:c.3928del ENSP00000359478.4:p.Arg1310AspfsTer?
NM_000392.4:c.3928del NP_000383.1:p.Arg1310AspfsTer?
XM_006717630.2:c.3232del XP_006717693.1:p.Arg1078AspfsTer?
XR_945604.1:n.4117del
XR_945605.1:n.3992del
NM_000392.5:c.3928del MANE Select NP_000383.2:p.Arg1310AspfsTer?
XM_006717630.3:c.3232del XP_006717693.1:p.Arg1078AspfsTer?
XR_945604.3:n.4171del
XR_945605.3:n.4044del
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