Canonical Allele Identifier: CA2610492376

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99782733-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99782734dup , CM000672.2:g.99782734dup	GRCh38
NC_000010.10:g.101542491dup , CM000672.1:g.101542491dup	GRCh37
NC_000010.9:g.101532481dup	NCBI36
NG_011798.1:g.5029dup
NG_011798.2:g.5137dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.-111dup MANE Select	ENSP00000497274.1:n.-111dup
ENST00000647836.1:n.95dup
ENST00000648324.1:c.-111dup	ENSP00000497248.1:n.-111dup
ENST00000648689.1:c.-111dup	ENSP00000496972.1:n.-111dup
ENST00000649932.1:c.-111dup	ENSP00000498120.1:n.-111dup
ENST00000370449.8:c.-111dup	ENSP00000359478.4:n.-111dup
NM_000392.4:c.-111dup	NP_000383.1:n.-111dup
XM_006717631.2:c.-111dup	XP_006717694.1:n.-111dup
XM_011539291.1:c.-111dup	XP_011537593.1:n.-111dup
XR_945604.1:n.79dup
XR_945605.1:n.81dup
NM_000392.5:c.-111dup MANE Select	NP_000383.2:n.-111dup
XM_006717631.4:c.-111dup	XP_006717694.1:n.-111dup
XM_011539291.3:c.-111dup	XP_011537593.1:n.-111dup
XM_017015675.2:c.-111dup	XP_016871164.1:n.-111dup
XR_945604.3:n.133dup
XR_945605.3:n.133dup