Canonical Allele Identifier: CA1931512179
Gene: ABCC2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844499C= , CM000672.2:g.99844499C= GRCh38
NC_000010.10:g.101604256C= , CM000672.1:g.101604256C= GRCh37
NC_000010.9:g.101594246C= NCBI36
NG_011798.1:g.66794C=
NG_011798.2:g.66902C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3987+34C= MANE Select ENSP00000497274.1:n.3987+34C=
ENST00000649459.1:n.335+34C=
ENST00000370449.8:c.3987+34C= ENSP00000359478.4:n.3987+34C=
NM_000392.4:c.3987+34C= NP_000383.1:n.3987+34C=
XM_006717630.2:c.3291+34C= XP_006717693.1:n.3291+34C=
XR_945604.1:n.4176+34C=
XR_945605.1:n.4051+34C=
NM_000392.5:c.3987+34C= MANE Select NP_000383.2:n.3987+34C=
XM_006717630.3:c.3291+34C= XP_006717693.1:n.3291+34C=
XR_945604.3:n.4230+34C=
XR_945605.3:n.4103+34C=
Search 100 bp 5'
Search 100 bp 3'