Canonical Allele Identifier: CA471131817
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101595883T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836126T>A , CM000672.2:g.99836126T>A GRCh38
NC_000010.10:g.101595883T>A , CM000672.1:g.101595883T>A GRCh37
NC_000010.9:g.101585873T>A NCBI36
NG_011798.1:g.58421T>A
NG_011798.2:g.58529T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3450T>A MANE Select ENSP00000497274.1:p.Arg1150=
ENST00000370449.8:c.3450T>A ENSP00000359478.4:p.Arg1150=
NM_000392.4:c.3450T>A NP_000383.1:p.Arg1150=
XM_006717630.2:c.2754T>A XP_006717693.1:p.Arg918=
XR_945604.1:n.3639T>A
XR_945605.1:n.3641T>A
NM_000392.5:c.3450T>A MANE Select NP_000383.2:p.Arg1150=
XM_006717630.3:c.2754T>A XP_006717693.1:p.Arg918=
XR_945604.3:n.3693T>A
XR_945605.3:n.3693T>A
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