Canonical Allele Identifier: CA5445950
Gene: GAD2 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.26245880G>T
GRCh37 chr10:g.26534809G>T
gnomAD v2:
10:26534809 G / T
gnomAD v3:
10:26245880 G / T
gnomAD v4:
chr10-26245880-G-T
Joint Max Group AF 0.33491784 (AFR)
Genomes Max Group AF 0.33348548 (AFR)
Exomes Max Group AF 0.33342054 (AFR)
dbSNP:
1805398
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26245880G>T , CM000672.2:g.26245880G>T GRCh38
NC_000010.10:g.26534809G>T , CM000672.1:g.26534809G>T GRCh37
NC_000010.9:g.26574815G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376261.8:c.841-41G>T MANE Select ENSP00000365437.3:n.841-41G>T
ENST00000648567.1:c.499-41G>T ENSP00000498009.1:n.499-41G>T
ENST00000259271.7:c.841-41G>T ENSP00000259271.3:n.841-41G>T
ENST00000376261.7:c.841-41G>T ENSP00000365437.3:n.841-41G>T
NM_000818.2:c.841-41G>T NP_000809.1:n.841-41G>T
NM_001134366.1:c.841-41G>T NP_001127838.1:n.841-41G>T
NM_001134366.2:c.841-41G>T MANE Select NP_001127838.1:n.841-41G>T
NM_000818.3:c.841-41G>T NP_000809.1:n.841-41G>T
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