Canonical Allele Identifier: CA537695005
Gene: GAD1 HGNC NCBI

Linked Data

dbSNP Id: rs1559262702
gnomAD v2: 2-171670655-ATGT-A
gnomAD v3: 2-170814145-ATGT-A
gnomAD v4: 2-170814145-ATGT-A
MyVariant Identifiers: chr2:g.171670656_171670658del (hg19) chr2:g.170814146_170814148del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.170814150_170814152del , CM000664.2:g.170814150_170814152del GRCh38
NC_000002.11:g.171670660_171670662del , CM000664.1:g.171670660_171670662del GRCh37
NC_000002.10:g.171378906_171378908del NCBI36
NG_021477.1:g.2461_2463del

Transcript Alleles

HGVS Amino-acid Change
ENST00000454603.5:c.-64+728_-64+730del ENSP00000402366.1:n.-64+728_-64+730del
XM_011510922.1:c.-64+728_-64+730del XP_011509224.1:n.-64+728_-64+730del
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