Canonical Allele Identifier: CA13139117

Gene: ADARB2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.1588626C>T , CM000672.2:g.1588626C>T	GRCh38
NC_000010.10:g.1630821C>T , CM000672.1:g.1630821C>T	GRCh37
NC_000010.9:g.1620821C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381312.6:c.100+148425G>A MANE Select	ENSP00000370713.1:n.100+148425G>A
ENST00000381312.5:c.100+148425G>A	ENSP00000370713.1:n.100+148425G>A
NM_018702.3:c.100+148425G>A	NP_061172.1:n.100+148425G>A
XR_930468.1:n.448+148425G>A
NM_018702.4:c.100+148425G>A MANE Select	NP_061172.1:n.100+148425G>A