Canonical Allele Identifier: CA1775819
Gene: ADRA2B HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.96114968T>A
GRCh37 chr2:g.96780716T>A
gnomAD v2:
2:96780716 T / A
gnomAD v3:
2:96114968 T / A
gnomAD v4:
chr2-96114968-T-A
Joint Max Group AF 0.00001745 (AFR)
Genomes Max Group AF 0.00000798 (AFR)
Exomes Max Group AF 0.0000099 (AFR)
dbSNP:
2229169
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96114968T>A , CM000664.2:g.96114968T>A GRCh38
NC_000002.11:g.96780716T>A , CM000664.1:g.96780716T>A GRCh37
NC_000002.10:g.96144443T>A NCBI36
NG_032950.1:g.6182A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000620793.2:c.1182A>T MANE Select ENSP00000480573.1:p.Gly394=
ENST00000620793.1:c.1182A>T ENSP00000480573.1:p.Gly394=
NM_000682.6:c.1182A>T NP_000673.2:p.Gly394=
NM_000682.7:c.1182A>T MANE Select NP_000673.2:p.Gly394=
Search 100 bp 5'
Search 100 bp 3'