Canonical Allele Identifier: CA212862447

Gene: ABCC2

Linked Data

• dbSNP Id: rs36042666

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836468dup , CM000672.2:g.99836468dup	GRCh38
NC_000010.10:g.101596225dup , CM000672.1:g.101596225dup	GRCh37
NC_000010.9:g.101586215dup	NCBI36
NG_011798.1:g.58763dup
NG_011798.2:g.58871dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3614+178dup MANE Select	ENSP00000497274.1:n.3614+178dup
ENST00000370449.8:c.3614+178dup	ENSP00000359478.4:n.3614+178dup
NM_000392.4:c.3614+178dup	NP_000383.1:n.3614+178dup
XM_006717630.2:c.2918+178dup	XP_006717693.1:n.2918+178dup
XR_945604.1:n.3803+178dup
XR_945605.1:n.3805+178dup
NM_000392.5:c.3614+178dup MANE Select	NP_000383.2:n.3614+178dup
XM_006717630.3:c.2918+178dup	XP_006717693.1:n.2918+178dup
XR_945604.3:n.3857+178dup
XR_945605.3:n.3857+178dup