Canonical Allele Identifier: CA378124504
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836155A>C , CM000672.2:g.99836155A>C GRCh38
NC_000010.10:g.101595912A>C , CM000672.1:g.101595912A>C GRCh37
NC_000010.9:g.101585902A>C NCBI36
NG_011798.1:g.58450A>C
NG_011798.2:g.58558A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3479A>C MANE Select ENSP00000497274.1:p.Tyr1160Ser
ENST00000370449.8:c.3479A>C ENSP00000359478.4:p.Tyr1160Ser
NM_000392.4:c.3479A>C NP_000383.1:p.Tyr1160Ser
XM_006717630.2:c.2783A>C XP_006717693.1:p.Tyr928Ser
XR_945604.1:n.3668A>C
XR_945605.1:n.3670A>C
NM_000392.5:c.3479A>C MANE Select NP_000383.2:p.Tyr1160Ser
XM_006717630.3:c.2783A>C XP_006717693.1:p.Tyr928Ser
XR_945604.3:n.3722A>C
XR_945605.3:n.3722A>C