Canonical Allele Identifier: CA931722494
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2039010524

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845942A>G , CM000672.2:g.99845942A>G GRCh38
NC_000010.10:g.101605699A>G , CM000672.1:g.101605699A>G GRCh37
NC_000010.9:g.101595689A>G NCBI36
NG_011798.1:g.68237A>G
NG_011798.2:g.68345A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146+160A>G MANE Select ENSP00000497274.1:n.4146+160A>G
ENST00000648523.1:c.34+160A>G
ENST00000649459.1:n.494+160A>G
ENST00000370449.8:c.4146+160A>G ENSP00000359478.4:n.4146+160A>G
NM_000392.4:c.4146+160A>G NP_000383.1:n.4146+160A>G
XM_006717630.2:c.3450+160A>G XP_006717693.1:n.3450+160A>G
XR_945604.1:n.4276+160A>G
XR_945605.1:n.4210+160A>G
NM_000392.5:c.4146+160A>G MANE Select NP_000383.2:n.4146+160A>G
XM_006717630.3:c.3450+160A>G XP_006717693.1:n.3450+160A>G
XR_945604.3:n.4330+160A>G
XR_945605.3:n.4262+160A>G