Canonical Allele Identifier: CA471132108
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101596039C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836282C>A , CM000672.2:g.99836282C>A GRCh38
NC_000010.10:g.101596039C>A , CM000672.1:g.101596039C>A GRCh37
NC_000010.9:g.101586029C>A NCBI36
NG_011798.1:g.58577C>A
NG_011798.2:g.58685C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3606C>A MANE Select ENSP00000497274.1:p.Thr1202=
ENST00000370449.8:c.3606C>A ENSP00000359478.4:p.Thr1202=
NM_000392.4:c.3606C>A NP_000383.1:p.Thr1202=
XM_006717630.2:c.2910C>A XP_006717693.1:p.Thr970=
XR_945604.1:n.3795C>A
XR_945605.1:n.3797C>A
NM_000392.5:c.3606C>A MANE Select NP_000383.2:p.Thr1202=
XM_006717630.3:c.2910C>A XP_006717693.1:p.Thr970=
XR_945604.3:n.3849C>A
XR_945605.3:n.3849C>A
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