Canonical Allele Identifier: CA2610497882
Gene: ABCC2 HGNC NCBI

Linked Data

gnomAD v4: 10-99845590-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845590G>A , CM000672.2:g.99845590G>A GRCh38
NC_000010.10:g.101605347G>A , CM000672.1:g.101605347G>A GRCh37
NC_000010.9:g.101595337G>A NCBI36
NG_011798.1:g.67885G>A
NG_011798.2:g.67993G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3988-34G>A MANE Select ENSP00000497274.1:n.3988-34G>A
ENST00000649459.1:n.336-34G>A
ENST00000370449.8:c.3988-34G>A ENSP00000359478.4:n.3988-34G>A
NM_000392.4:c.3988-34G>A NP_000383.1:n.3988-34G>A
XM_006717630.2:c.3292-34G>A XP_006717693.1:n.3292-34G>A
XR_945604.1:n.4177-93G>A
XR_945605.1:n.4052-34G>A
NM_000392.5:c.3988-34G>A MANE Select NP_000383.2:n.3988-34G>A
XM_006717630.3:c.3292-34G>A XP_006717693.1:n.3292-34G>A
XR_945604.3:n.4231-93G>A
XR_945605.3:n.4104-34G>A
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