Canonical Allele Identifier: CA213922427
Gene: ADRA2A HGNC NCBI

Linked Data

dbSNP Id: rs1016205043
gnomAD v4: 10-111079639-T-A
MyVariant Identifiers: chr10:g.112839397T>A (hg19) chr10:g.111079639T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.111079639T>A , CM000672.2:g.111079639T>A GRCh38
NC_000010.10:g.112839397T>A , CM000672.1:g.112839397T>A GRCh37
NC_000010.9:g.112829387T>A NCBI36
NG_012020.1:g.7608T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000280155.4:c.*245T>A MANE Select ENSP00000280155.2:n.*245T>A
ENST00000280155.3:c.*245T>A ENSP00000280155.2:n.*245T>A
NM_000681.3:c.*245T>A NP_000672.3:n.*245T>A
NM_000681.4:c.*245T>A MANE Select NP_000672.3:n.*245T>A
Search 100 bp 5'
Search 100 bp 3'