Canonical Allele Identifier: CA378126660
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844334A>T , CM000672.2:g.99844334A>T GRCh38
NC_000010.10:g.101604091A>T , CM000672.1:g.101604091A>T GRCh37
NC_000010.9:g.101594081A>T NCBI36
NG_011798.1:g.66629A>T
NG_011798.2:g.66737A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3856A>T MANE Select ENSP00000497274.1:p.Thr1286Ser
ENST00000649459.1:n.204A>T
ENST00000370449.8:c.3856A>T ENSP00000359478.4:p.Thr1286Ser
NM_000392.4:c.3856A>T NP_000383.1:p.Thr1286Ser
XM_006717630.2:c.3160A>T XP_006717693.1:p.Thr1054Ser
XR_945604.1:n.4045A>T
XR_945605.1:n.3920A>T
NM_000392.5:c.3856A>T MANE Select NP_000383.2:p.Thr1286Ser
XM_006717630.3:c.3160A>T XP_006717693.1:p.Thr1054Ser
XR_945604.3:n.4099A>T
XR_945605.3:n.3972A>T