Canonical Allele Identifier: CA278794
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs864309675
MyVariant Identifiers: chr10:g.101559109_101559110del (hg19) chr10:g.99799352_99799353del (hg38)
PubMed: PMID:26350512
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99799352_99799353del , CM000672.2:g.99799352_99799353del GRCh38
NC_000010.10:g.101559109_101559110del , CM000672.1:g.101559109_101559110del GRCh37
NC_000010.9:g.101549099_101549100del NCBI36
NG_011798.1:g.21647_21648del
NG_011798.2:g.21755_21756del

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.1013_1014del MANE Select ENSP00000497274.1:p.Val338GlufsTer14
ENST00000370449.8:c.1013_1014del ENSP00000359478.4:p.Val338GlufsTer14
NM_000392.4:c.1013_1014del NP_000383.1:p.Val338GlufsTer14
XM_006717630.2:c.317_318del XP_006717693.1:p.Val106GlufsTer14
XM_006717631.2:c.1013_1014del XP_006717694.1:p.Val338GlufsTer14
XM_011539291.1:c.1013_1014del XP_011537593.1:p.Val338GlufsTer14
XR_945604.1:n.1202_1203del
XR_945605.1:n.1204_1205del
NM_000392.5:c.1013_1014del MANE Select NP_000383.2:p.Val338GlufsTer14
XM_006717630.3:c.317_318del XP_006717693.1:p.Val106GlufsTer14
XM_006717631.4:c.1013_1014del XP_006717694.1:p.Val338GlufsTer14
XM_011539291.3:c.1013_1014del XP_011537593.1:p.Val338GlufsTer14
XM_017015675.2:c.1013_1014del XP_016871164.1:p.Val338GlufsTer14
XR_945604.3:n.1256_1257del
XR_945605.3:n.1256_1257del
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