Canonical Allele Identifier: CA378126664
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844335C>G , CM000672.2:g.99844335C>G GRCh38
NC_000010.10:g.101604092C>G , CM000672.1:g.101604092C>G GRCh37
NC_000010.9:g.101594082C>G NCBI36
NG_011798.1:g.66630C>G
NG_011798.2:g.66738C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3857C>G MANE Select ENSP00000497274.1:p.Thr1286Ser
ENST00000649459.1:n.205C>G
ENST00000370449.8:c.3857C>G ENSP00000359478.4:p.Thr1286Ser
NM_000392.4:c.3857C>G NP_000383.1:p.Thr1286Ser
XM_006717630.2:c.3161C>G XP_006717693.1:p.Thr1054Ser
XR_945604.1:n.4046C>G
XR_945605.1:n.3921C>G
NM_000392.5:c.3857C>G MANE Select NP_000383.2:p.Thr1286Ser
XM_006717630.3:c.3161C>G XP_006717693.1:p.Thr1054Ser
XR_945604.3:n.4100C>G
XR_945605.3:n.3973C>G