Canonical Allele Identifier: CA1931484411
Gene: ABCC2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99851378A= , CM000672.2:g.99851378A= GRCh38
NC_000010.10:g.101611135A= , CM000672.1:g.101611135A= GRCh37
NC_000010.9:g.101601125A= NCBI36
NG_011798.1:g.73673A=
NG_011798.2:g.73781A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.4509-124A= MANE Select ENSP00000497274.1:n.4509-124A=
ENST00000648523.1:c.579-124A=
ENST00000370449.8:c.4509-124A= ENSP00000359478.4:n.4509-124A=
NM_000392.4:c.4509-124A= NP_000383.1:n.4509-124A=
XM_006717630.2:c.3813-124A= XP_006717693.1:n.3813-124A=
XR_945605.1:n.4573-124A=
NM_000392.5:c.4509-124A= MANE Select NP_000383.2:n.4509-124A=
XM_006717630.3:c.3813-124A= XP_006717693.1:n.3813-124A=
XR_945605.3:n.4625-124A=
Search 100 bp 5'
Search 100 bp 3'