Canonical Allele Identifier: CA1931512424
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844662_99844663delinsGC , CM000672.2:g.99844662_99844663delinsGC GRCh38
NC_000010.10:g.101604419_101604420delinsGC , CM000672.1:g.101604419_101604420delinsGC GRCh37
NC_000010.9:g.101594409_101594410delinsGC NCBI36
NG_011798.1:g.66957_66958delinsGC
NG_011798.2:g.67065_67066delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3987+197_3987+198delinsGC MANE Select ENSP00000497274.1:n.3987+197_3987+198delinsGC
ENST00000649459.1:n.335+197_335+198delinsGC
ENST00000370449.8:c.3987+197_3987+198delinsGC ENSP00000359478.4:n.3987+197_3987+198delinsGC
NM_000392.4:c.3987+197_3987+198delinsGC NP_000383.1:n.3987+197_3987+198delinsGC
XM_006717630.2:c.3291+197_3291+198delinsGC XP_006717693.1:n.3291+197_3291+198delinsGC
XR_945604.1:n.4176+197_4176+198delinsGC
XR_945605.1:n.4051+197_4051+198delinsGC
NM_000392.5:c.3987+197_3987+198delinsGC MANE Select NP_000383.2:n.3987+197_3987+198delinsGC
XM_006717630.3:c.3291+197_3291+198delinsGC XP_006717693.1:n.3291+197_3291+198delinsGC
XR_945604.3:n.4230+197_4230+198delinsGC
XR_945605.3:n.4103+197_4103+198delinsGC