Canonical Allele Identifier: CA2610497278

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99836336-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836340_99836341del , CM000672.2:g.99836340_99836341del	GRCh38
NC_000010.10:g.101596097_101596098del , CM000672.1:g.101596097_101596098del	GRCh37
NC_000010.9:g.101586087_101586088del	NCBI36
NG_011798.1:g.58635_58636del
NG_011798.2:g.58743_58744del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3614+50_3614+51del MANE Select	ENSP00000497274.1:n.3614+50_3614+51del
ENST00000370449.8:c.3614+50_3614+51del	ENSP00000359478.4:n.3614+50_3614+51del
NM_000392.4:c.3614+50_3614+51del	NP_000383.1:n.3614+50_3614+51del
XM_006717630.2:c.2918+50_2918+51del	XP_006717693.1:n.2918+50_2918+51del
XR_945604.1:n.3803+50_3803+51del
XR_945605.1:n.3805+50_3805+51del
NM_000392.5:c.3614+50_3614+51del MANE Select	NP_000383.2:n.3614+50_3614+51del
XM_006717630.3:c.2918+50_2918+51del	XP_006717693.1:n.2918+50_2918+51del
XR_945604.3:n.3857+50_3857+51del
XR_945605.3:n.3857+50_3857+51del