Canonical Allele Identifier: CA2589023846
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1222877158
gnomAD v3: 10-99845989-G-A
gnomAD v4: 10-99845989-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845989G>A , CM000672.2:g.99845989G>A GRCh38
NC_000010.10:g.101605746G>A , CM000672.1:g.101605746G>A GRCh37
NC_000010.9:g.101595736G>A NCBI36
NG_011798.1:g.68284G>A
NG_011798.2:g.68392G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146+207G>A MANE Select ENSP00000497274.1:n.4146+207G>A
ENST00000648523.1:c.34+207G>A
ENST00000649459.1:n.494+207G>A
ENST00000370449.8:c.4146+207G>A ENSP00000359478.4:n.4146+207G>A
NM_000392.4:c.4146+207G>A NP_000383.1:n.4146+207G>A
XM_006717630.2:c.3450+207G>A XP_006717693.1:n.3450+207G>A
XR_945604.1:n.4276+207G>A
XR_945605.1:n.4210+207G>A
NM_000392.5:c.4146+207G>A MANE Select NP_000383.2:n.4146+207G>A
XM_006717630.3:c.3450+207G>A XP_006717693.1:n.3450+207G>A
XR_945604.3:n.4330+207G>A
XR_945605.3:n.4262+207G>A
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