Canonical Allele Identifier: CA2610497843

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845515-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845515A>G , CM000672.2:g.99845515A>G	GRCh38
NC_000010.10:g.101605272A>G , CM000672.1:g.101605272A>G	GRCh37
NC_000010.9:g.101595262A>G	NCBI36
NG_011798.1:g.67810A>G
NG_011798.2:g.67918A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3988-109A>G MANE Select	ENSP00000497274.1:n.3988-109A>G
ENST00000649459.1:n.336-109A>G
ENST00000370449.8:c.3988-109A>G	ENSP00000359478.4:n.3988-109A>G
NM_000392.4:c.3988-109A>G	NP_000383.1:n.3988-109A>G
XM_006717630.2:c.3292-109A>G	XP_006717693.1:n.3292-109A>G
XR_945604.1:n.4177-168A>G
XR_945605.1:n.4052-109A>G
NM_000392.5:c.3988-109A>G MANE Select	NP_000383.2:n.3988-109A>G
XM_006717630.3:c.3292-109A>G	XP_006717693.1:n.3292-109A>G
XR_945604.3:n.4231-168A>G
XR_945605.3:n.4104-109A>G