Canonical Allele Identifier: CA378125080
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836251C>T , CM000672.2:g.99836251C>T GRCh38
NC_000010.10:g.101596008C>T , CM000672.1:g.101596008C>T GRCh37
NC_000010.9:g.101585998C>T NCBI36
NG_011798.1:g.58546C>T
NG_011798.2:g.58654C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3575C>T MANE Select ENSP00000497274.1:p.Thr1192Ile
ENST00000370449.8:c.3575C>T ENSP00000359478.4:p.Thr1192Ile
NM_000392.4:c.3575C>T NP_000383.1:p.Thr1192Ile
XM_006717630.2:c.2879C>T XP_006717693.1:p.Thr960Ile
XR_945604.1:n.3764C>T
XR_945605.1:n.3766C>T
NM_000392.5:c.3575C>T MANE Select NP_000383.2:p.Thr1192Ile
XM_006717630.3:c.2879C>T XP_006717693.1:p.Thr960Ile
XR_945604.3:n.3818C>T
XR_945605.3:n.3818C>T