Canonical Allele Identifier: CA1931496729
Gene: ABCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836458A= , CM000672.2:g.99836458A= GRCh38
NC_000010.10:g.101596215A= , CM000672.1:g.101596215A= GRCh37
NC_000010.9:g.101586205A= NCBI36
NG_011798.1:g.58753A=
NG_011798.2:g.58861A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3614+168A= MANE Select ENSP00000497274.1:n.3614+168A=
ENST00000370449.8:c.3614+168A= ENSP00000359478.4:n.3614+168A=
NM_000392.4:c.3614+168A= NP_000383.1:n.3614+168A=
XM_006717630.2:c.2918+168A= XP_006717693.1:n.2918+168A=
XR_945604.1:n.3803+168A=
XR_945605.1:n.3805+168A=
NM_000392.5:c.3614+168A= MANE Select NP_000383.2:n.3614+168A=
XM_006717630.3:c.2918+168A= XP_006717693.1:n.2918+168A=
XR_945604.3:n.3857+168A=
XR_945605.3:n.3857+168A=
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