Canonical Allele Identifier: CA1931512196
Gene: ABCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844512C= , CM000672.2:g.99844512C= GRCh38
NC_000010.10:g.101604269C= , CM000672.1:g.101604269C= GRCh37
NC_000010.9:g.101594259C= NCBI36
NG_011798.1:g.66807C=
NG_011798.2:g.66915C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3987+47C= MANE Select ENSP00000497274.1:n.3987+47C=
ENST00000649459.1:n.335+47C=
ENST00000370449.8:c.3987+47C= ENSP00000359478.4:n.3987+47C=
NM_000392.4:c.3987+47C= NP_000383.1:n.3987+47C=
XM_006717630.2:c.3291+47C= XP_006717693.1:n.3291+47C=
XR_945604.1:n.4176+47C=
XR_945605.1:n.4051+47C=
NM_000392.5:c.3987+47C= MANE Select NP_000383.2:n.3987+47C=
XM_006717630.3:c.3291+47C= XP_006717693.1:n.3291+47C=
XR_945604.3:n.4230+47C=
XR_945605.3:n.4103+47C=
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