Canonical Allele Identifier: CA1931491764
Community Standard Title: NM_000392.5(ABCC2):c.3258+56T=
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99832187T= , CM000672.2:g.99832187T= GRCh38
NC_000010.10:g.101591944T= , CM000672.1:g.101591944T= GRCh37
NC_000010.9:g.101581934T= NCBI36
NG_011798.1:g.54482T=
NG_011798.2:g.54590T=

Transcript Alleles

HGVS Amino-acid Change
NM_000392.5:c.3258+56T= MANE Select NP_000383.2:n.3258+56T=
ENST00000647814.1:c.3258+56T= MANE Select ENSP00000497274.1:n.3258+56T=
NM_000392.4:c.3258+56T= NP_000383.1:n.3258+56T=
ENST00000370449.8:c.3258+56T= ENSP00000359478.4:n.3258+56T=
XM_006717630.2:c.2562+56T= XP_006717693.1:n.2562+56T=
XM_006717630.3:c.2562+56T= XP_006717693.1:n.2562+56T=
XR_945604.1:n.3447+56T=
XR_945604.3:n.3501+56T=
XR_945605.1:n.3449+56T=
XR_945605.3:n.3501+56T=