Canonical Allele Identifier: CA760613693
Gene: GAD1 HGNC NCBI

Linked Data

dbSNP Id: rs1307460266
gnomAD v3: 2-170814260-CTGT-C
gnomAD v4: 2-170814260-CTGT-C
MyVariant Identifiers: chr2:g.171670771_171670773del (hg19) chr2:g.170814261_170814263del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.170814261_170814263del , CM000664.2:g.170814261_170814263del GRCh38
NC_000002.11:g.171670771_171670773del , CM000664.1:g.171670771_171670773del GRCh37
NC_000002.10:g.171379017_171379019del NCBI36
NG_021477.1:g.2572_2574del

Transcript Alleles

HGVS Amino-acid Change
ENST00000454603.5:c.-64+839_-64+841del ENSP00000402366.1:n.-64+839_-64+841del
XM_011510922.1:c.-64+839_-64+841del XP_011509224.1:n.-64+839_-64+841del
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