Canonical Allele Identifier: CA213922426
Gene: ADRA2A HGNC NCBI

Linked Data

dbSNP Id: rs538266316
gnomAD v2: 10-112839385-C-T
gnomAD v3: 10-111079627-C-T
gnomAD v4: 10-111079627-C-T
MyVariant Identifiers: chr10:g.112839385C>T (hg19) chr10:g.111079627C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.111079627C>T , CM000672.2:g.111079627C>T GRCh38
NC_000010.10:g.112839385C>T , CM000672.1:g.112839385C>T GRCh37
NC_000010.9:g.112829375C>T NCBI36
NG_012020.1:g.7596C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000280155.4:c.*233C>T MANE Select ENSP00000280155.2:n.*233C>T
ENST00000280155.3:c.*233C>T ENSP00000280155.2:n.*233C>T
NM_000681.3:c.*233C>T NP_000672.3:n.*233C>T
NM_000681.4:c.*233C>T MANE Select NP_000672.3:n.*233C>T
Search 100 bp 5'
Search 100 bp 3'