Canonical Allele Identifier: CA378116437
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101577095T>A (hg19) chr10:g.99817338T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99817338T>A , CM000672.2:g.99817338T>A GRCh38
NC_000010.10:g.101577095T>A , CM000672.1:g.101577095T>A GRCh37
NC_000010.9:g.101567085T>A NCBI36
NG_011798.1:g.39633T>A
NG_011798.2:g.39741T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.2125T>A MANE Select ENSP00000497274.1:p.Trp709Arg
ENST00000370449.8:c.2125T>A ENSP00000359478.4:p.Trp709Arg
NM_000392.4:c.2125T>A NP_000383.1:p.Trp709Arg
XM_006717630.2:c.1429T>A XP_006717693.1:p.Trp477Arg
XM_006717631.2:c.2125T>A XP_006717694.1:p.Trp709Arg
XM_011539291.1:c.2125T>A XP_011537593.1:p.Trp709Arg
XR_945604.1:n.2314T>A
XR_945605.1:n.2316T>A
NM_000392.5:c.2125T>A MANE Select NP_000383.2:p.Trp709Arg
XM_006717630.3:c.1429T>A XP_006717693.1:p.Trp477Arg
XM_006717631.4:c.2125T>A XP_006717694.1:p.Trp709Arg
XM_011539291.3:c.2125T>A XP_011537593.1:p.Trp709Arg
XM_017015675.2:c.2125T>A XP_016871164.1:p.Trp709Arg
XR_945604.3:n.2368T>A
XR_945605.3:n.2368T>A
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