Canonical Allele Identifier: CA378125181
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836271T>G , CM000672.2:g.99836271T>G GRCh38
NC_000010.10:g.101596028T>G , CM000672.1:g.101596028T>G GRCh37
NC_000010.9:g.101586018T>G NCBI36
NG_011798.1:g.58566T>G
NG_011798.2:g.58674T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3595T>G MANE Select ENSP00000497274.1:p.Ser1199Ala
ENST00000370449.8:c.3595T>G ENSP00000359478.4:p.Ser1199Ala
NM_000392.4:c.3595T>G NP_000383.1:p.Ser1199Ala
XM_006717630.2:c.2899T>G XP_006717693.1:p.Ser967Ala
XR_945604.1:n.3784T>G
XR_945605.1:n.3786T>G
NM_000392.5:c.3595T>G MANE Select NP_000383.2:p.Ser1199Ala
XM_006717630.3:c.2899T>G XP_006717693.1:p.Ser967Ala
XR_945604.3:n.3838T>G
XR_945605.3:n.3838T>G