Canonical Allele Identifier: CA1931512436
Gene: ABCC2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844670C= , CM000672.2:g.99844670C= GRCh38
NC_000010.10:g.101604427C= , CM000672.1:g.101604427C= GRCh37
NC_000010.9:g.101594417C= NCBI36
NG_011798.1:g.66965C=
NG_011798.2:g.67073C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3987+205C= MANE Select ENSP00000497274.1:n.3987+205C=
ENST00000649459.1:n.335+205C=
ENST00000370449.8:c.3987+205C= ENSP00000359478.4:n.3987+205C=
NM_000392.4:c.3987+205C= NP_000383.1:n.3987+205C=
XM_006717630.2:c.3291+205C= XP_006717693.1:n.3291+205C=
XR_945604.1:n.4176+205C=
XR_945605.1:n.4051+205C=
NM_000392.5:c.3987+205C= MANE Select NP_000383.2:n.3987+205C=
XM_006717630.3:c.3291+205C= XP_006717693.1:n.3291+205C=
XR_945604.3:n.4230+205C=
XR_945605.3:n.4103+205C=
Search 100 bp 5'
Search 100 bp 3'