Canonical Allele Identifier: CA471135618
Gene: ABCC2 HGNC NCBI

Linked Data

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

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

Transcript Alleles

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