Canonical Allele Identifier: CA2610497730
Gene: ABCC2 HGNC NCBI

Linked Data

gnomAD v4: 10-99844473-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844473G>A , CM000672.2:g.99844473G>A GRCh38
NC_000010.10:g.101604230G>A , CM000672.1:g.101604230G>A GRCh37
NC_000010.9:g.101594220G>A NCBI36
NG_011798.1:g.66768G>A
NG_011798.2:g.66876G>A

Transcript Alleles

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