Canonical Allele Identifier: CA1931484447
Gene: ABCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99851391G= , CM000672.2:g.99851391G= GRCh38
NC_000010.10:g.101611148G= , CM000672.1:g.101611148G= GRCh37
NC_000010.9:g.101601138G= NCBI36
NG_011798.1:g.73686G=
NG_011798.2:g.73794G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.4509-111G= MANE Select ENSP00000497274.1:n.4509-111G=
ENST00000648523.1:c.579-111G=
ENST00000370449.8:c.4509-111G= ENSP00000359478.4:n.4509-111G=
NM_000392.4:c.4509-111G= NP_000383.1:n.4509-111G=
XM_006717630.2:c.3813-111G= XP_006717693.1:n.3813-111G=
XR_945605.1:n.4573-111G=
NM_000392.5:c.4509-111G= MANE Select NP_000383.2:n.4509-111G=
XM_006717630.3:c.3813-111G= XP_006717693.1:n.3813-111G=
XR_945605.3:n.4625-111G=
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