Canonical Allele Identifier: CA378128550
Gene: ABCC2 HGNC NCBI

Linked Data

gnomAD v4: 10-99845781-A-C
MyVariant Identifiers: chr10:g.101605538A>C (hg19) chr10:g.99845781A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845781A>C , CM000672.2:g.99845781A>C GRCh38
NC_000010.10:g.101605538A>C , CM000672.1:g.101605538A>C GRCh37
NC_000010.9:g.101595528A>C NCBI36
NG_011798.1:g.68076A>C
NG_011798.2:g.68184A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4145A>C MANE Select ENSP00000497274.1:p.Gln1382Pro
ENST00000648523.1:c.33A>C
ENST00000649459.1:n.493A>C
ENST00000370449.8:c.4145A>C ENSP00000359478.4:p.Gln1382Pro
NM_000392.4:c.4145A>C NP_000383.1:p.Gln1382Pro
XM_006717630.2:c.3449A>C XP_006717693.1:p.Gln1150Pro
XR_945604.1:n.4275A>C
XR_945605.1:n.4209A>C
NM_000392.5:c.4145A>C MANE Select NP_000383.2:p.Gln1382Pro
XM_006717630.3:c.3449A>C XP_006717693.1:p.Gln1150Pro
XR_945604.3:n.4329A>C
XR_945605.3:n.4261A>C
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