Canonical Allele Identifier: CA378130485
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101611258G>A (hg19) chr10:g.99851501G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99851501G>A , CM000672.2:g.99851501G>A GRCh38
NC_000010.10:g.101611258G>A , CM000672.1:g.101611258G>A GRCh37
NC_000010.9:g.101601248G>A NCBI36
NG_011798.1:g.73796G>A
NG_011798.2:g.73904G>A

Transcript Alleles

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