Canonical Allele Identifier: CA2610497842
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845517_99845519dup , CM000672.2:g.99845517_99845519dup GRCh38
NC_000010.10:g.101605274_101605276dup , CM000672.1:g.101605274_101605276dup GRCh37
NC_000010.9:g.101595264_101595266dup NCBI36
NG_011798.1:g.67812_67814dup
NG_011798.2:g.67920_67922dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3988-107_3988-105dup MANE Select ENSP00000497274.1:n.3988-107_3988-105dup
ENST00000649459.1:n.336-107_336-105dup
ENST00000370449.8:c.3988-107_3988-105dup ENSP00000359478.4:n.3988-107_3988-105dup
NM_000392.4:c.3988-107_3988-105dup NP_000383.1:n.3988-107_3988-105dup
XM_006717630.2:c.3292-107_3292-105dup XP_006717693.1:n.3292-107_3292-105dup
XR_945604.1:n.4177-166_4177-164dup
XR_945605.1:n.4052-107_4052-105dup
NM_000392.5:c.3988-107_3988-105dup MANE Select NP_000383.2:n.3988-107_3988-105dup
XM_006717630.3:c.3292-107_3292-105dup XP_006717693.1:n.3292-107_3292-105dup
XR_945604.3:n.4231-166_4231-164dup
XR_945605.3:n.4104-107_4104-105dup