Canonical Allele Identifier: CA1931495698
Gene: ABCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99835740T= , CM000672.2:g.99835740T= GRCh38
NC_000010.10:g.101595497T= , CM000672.1:g.101595497T= GRCh37
NC_000010.9:g.101585487T= NCBI36
NG_011798.1:g.58035T=
NG_011798.2:g.58143T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3415-351T= MANE Select ENSP00000497274.1:n.3415-351T=
ENST00000370449.8:c.3415-351T= ENSP00000359478.4:n.3415-351T=
NM_000392.4:c.3415-351T= NP_000383.1:n.3415-351T=
XM_006717630.2:c.2719-351T= XP_006717693.1:n.2719-351T=
XR_945604.1:n.3604-351T=
XR_945605.1:n.3606-351T=
NM_000392.5:c.3415-351T= MANE Select NP_000383.2:n.3415-351T=
XM_006717630.3:c.2719-351T= XP_006717693.1:n.2719-351T=
XR_945604.3:n.3658-351T=
XR_945605.3:n.3658-351T=
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