Canonical Allele Identifier: CA471132096
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101596030C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836273C>A , CM000672.2:g.99836273C>A GRCh38
NC_000010.10:g.101596030C>A , CM000672.1:g.101596030C>A GRCh37
NC_000010.9:g.101586020C>A NCBI36
NG_011798.1:g.58568C>A
NG_011798.2:g.58676C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3597C>A MANE Select ENSP00000497274.1:p.Ser1199=
ENST00000370449.8:c.3597C>A ENSP00000359478.4:p.Ser1199=
NM_000392.4:c.3597C>A NP_000383.1:p.Ser1199=
XM_006717630.2:c.2901C>A XP_006717693.1:p.Ser967=
XR_945604.1:n.3786C>A
XR_945605.1:n.3788C>A
NM_000392.5:c.3597C>A MANE Select NP_000383.2:p.Ser1199=
XM_006717630.3:c.2901C>A XP_006717693.1:p.Ser967=
XR_945604.3:n.3840C>A
XR_945605.3:n.3840C>A
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