Canonical Allele Identifier: CA471135619
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101605458T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845701T>C , CM000672.2:g.99845701T>C GRCh38
NC_000010.10:g.101605458T>C , CM000672.1:g.101605458T>C GRCh37
NC_000010.9:g.101595448T>C NCBI36
NG_011798.1:g.67996T>C
NG_011798.2:g.68104T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4065T>C MANE Select ENSP00000497274.1:p.Gly1355=
ENST00000649459.1:n.413T>C
ENST00000370449.8:c.4065T>C ENSP00000359478.4:p.Gly1355=
NM_000392.4:c.4065T>C NP_000383.1:p.Gly1355=
XM_006717630.2:c.3369T>C XP_006717693.1:p.Gly1123=
XR_945604.1:n.4195T>C
XR_945605.1:n.4129T>C
NM_000392.5:c.4065T>C MANE Select NP_000383.2:p.Gly1355=
XM_006717630.3:c.3369T>C XP_006717693.1:p.Gly1123=
XR_945604.3:n.4249T>C
XR_945605.3:n.4181T>C
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