Canonical Allele Identifier: CA2610497885
Gene: ABCC2 HGNC NCBI

Linked Data

gnomAD v4: 10-99845596-CTAA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845598_99845600del , CM000672.2:g.99845598_99845600del GRCh38
NC_000010.10:g.101605355_101605357del , CM000672.1:g.101605355_101605357del GRCh37
NC_000010.9:g.101595345_101595347del NCBI36
NG_011798.1:g.67893_67895del
NG_011798.2:g.68001_68003del

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3988-26_3988-24del MANE Select ENSP00000497274.1:n.3988-26_3988-24del
ENST00000649459.1:n.336-26_336-24del
ENST00000370449.8:c.3988-26_3988-24del ENSP00000359478.4:n.3988-26_3988-24del
NM_000392.4:c.3988-26_3988-24del NP_000383.1:n.3988-26_3988-24del
XM_006717630.2:c.3292-26_3292-24del XP_006717693.1:n.3292-26_3292-24del
XR_945604.1:n.4177-85_4177-83del
XR_945605.1:n.4052-26_4052-24del
NM_000392.5:c.3988-26_3988-24del MANE Select NP_000383.2:n.3988-26_3988-24del
XM_006717630.3:c.3292-26_3292-24del XP_006717693.1:n.3292-26_3292-24del
XR_945604.3:n.4231-85_4231-83del
XR_945605.3:n.4104-26_4104-24del
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