Canonical Allele Identifier: CA378128050
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845685T>C , CM000672.2:g.99845685T>C GRCh38
NC_000010.10:g.101605442T>C , CM000672.1:g.101605442T>C GRCh37
NC_000010.9:g.101595432T>C NCBI36
NG_011798.1:g.67980T>C
NG_011798.2:g.68088T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.4049T>C MANE Select ENSP00000497274.1:p.Ile1350Thr
ENST00000649459.1:n.397T>C
ENST00000370449.8:c.4049T>C ENSP00000359478.4:p.Ile1350Thr
NM_000392.4:c.4049T>C NP_000383.1:p.Ile1350Thr
XM_006717630.2:c.3353T>C XP_006717693.1:p.Ile1118Thr
XR_945604.1:n.4179T>C
XR_945605.1:n.4113T>C
NM_000392.5:c.4049T>C MANE Select NP_000383.2:p.Ile1350Thr
XM_006717630.3:c.3353T>C XP_006717693.1:p.Ile1118Thr
XR_945604.3:n.4233T>C
XR_945605.3:n.4165T>C