Canonical Allele Identifier: CA1931512372
Gene: ABCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844643G= , CM000672.2:g.99844643G= GRCh38
NC_000010.10:g.101604400G= , CM000672.1:g.101604400G= GRCh37
NC_000010.9:g.101594390G= NCBI36
NG_011798.1:g.66938G=
NG_011798.2:g.67046G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3987+178G= MANE Select ENSP00000497274.1:n.3987+178G=
ENST00000649459.1:n.335+178G=
ENST00000370449.8:c.3987+178G= ENSP00000359478.4:n.3987+178G=
NM_000392.4:c.3987+178G= NP_000383.1:n.3987+178G=
XM_006717630.2:c.3291+178G= XP_006717693.1:n.3291+178G=
XR_945604.1:n.4176+178G=
XR_945605.1:n.4051+178G=
NM_000392.5:c.3987+178G= MANE Select NP_000383.2:n.3987+178G=
XM_006717630.3:c.3291+178G= XP_006717693.1:n.3291+178G=
XR_945604.3:n.4230+178G=
XR_945605.3:n.4103+178G=
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