Canonical Allele Identifier: CA2610497265

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99836296-G-GCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836298_99836300dup , CM000672.2:g.99836298_99836300dup	GRCh38
NC_000010.10:g.101596055_101596057dup , CM000672.1:g.101596055_101596057dup	GRCh37
NC_000010.9:g.101586045_101586047dup	NCBI36
NG_011798.1:g.58593_58595dup
NG_011798.2:g.58701_58703dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3614+8_3614+10dup MANE Select	ENSP00000497274.1:n.3614+8_3614+10dup
ENST00000370449.8:c.3614+8_3614+10dup	ENSP00000359478.4:n.3614+8_3614+10dup
NM_000392.4:c.3614+8_3614+10dup	NP_000383.1:n.3614+8_3614+10dup
XM_006717630.2:c.2918+8_2918+10dup	XP_006717693.1:n.2918+8_2918+10dup
XR_945604.1:n.3803+8_3803+10dup
XR_945605.1:n.3805+8_3805+10dup
NM_000392.5:c.3614+8_3614+10dup MANE Select	NP_000383.2:n.3614+8_3614+10dup
XM_006717630.3:c.2918+8_2918+10dup	XP_006717693.1:n.2918+8_2918+10dup
XR_945604.3:n.3857+8_3857+10dup
XR_945605.3:n.3857+8_3857+10dup