Canonical Allele Identifier: CA1931512326
Gene: ABCC2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844610G= , CM000672.2:g.99844610G= GRCh38
NC_000010.10:g.101604367G= , CM000672.1:g.101604367G= GRCh37
NC_000010.9:g.101594357G= NCBI36
NG_011798.1:g.66905G=
NG_011798.2:g.67013G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3987+145G= MANE Select ENSP00000497274.1:n.3987+145G=
ENST00000649459.1:n.335+145G=
ENST00000370449.8:c.3987+145G= ENSP00000359478.4:n.3987+145G=
NM_000392.4:c.3987+145G= NP_000383.1:n.3987+145G=
XM_006717630.2:c.3291+145G= XP_006717693.1:n.3291+145G=
XR_945604.1:n.4176+145G=
XR_945605.1:n.4051+145G=
NM_000392.5:c.3987+145G= MANE Select NP_000383.2:n.3987+145G=
XM_006717630.3:c.3291+145G= XP_006717693.1:n.3291+145G=
XR_945604.3:n.4230+145G=
XR_945605.3:n.4103+145G=
Search 100 bp 5'
Search 100 bp 3'