Canonical Allele Identifier: CA2610497886
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845600T>G , CM000672.2:g.99845600T>G GRCh38
NC_000010.10:g.101605357T>G , CM000672.1:g.101605357T>G GRCh37
NC_000010.9:g.101595347T>G NCBI36
NG_011798.1:g.67895T>G
NG_011798.2:g.68003T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3988-24T>G MANE Select ENSP00000497274.1:n.3988-24T>G
ENST00000649459.1:n.336-24T>G
ENST00000370449.8:c.3988-24T>G ENSP00000359478.4:n.3988-24T>G
NM_000392.4:c.3988-24T>G NP_000383.1:n.3988-24T>G
XM_006717630.2:c.3292-24T>G XP_006717693.1:n.3292-24T>G
XR_945604.1:n.4177-83T>G
XR_945605.1:n.4052-24T>G
NM_000392.5:c.3988-24T>G MANE Select NP_000383.2:n.3988-24T>G
XM_006717630.3:c.3292-24T>G XP_006717693.1:n.3292-24T>G
XR_945604.3:n.4231-83T>G
XR_945605.3:n.4104-24T>G