Canonical Allele Identifier: CA15179919
Gene: GAD1 HGNC NCBI

Linked Data

dbSNP Id: rs3762560
gnomAD v2: 2-171670863-A-G
gnomAD v3: 2-170814353-A-G
gnomAD v4: 2-170814353-A-G
MyVariant Identifiers: chr2:g.171670863A>G (hg19) chr2:g.170814353A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.170814353A>G , CM000664.2:g.170814353A>G GRCh38
NC_000002.11:g.171670863A>G , CM000664.1:g.171670863A>G GRCh37
NC_000002.10:g.171379109A>G NCBI36
NG_021477.1:g.2664A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000454603.5:c.-64+931A>G ENSP00000402366.1:n.-64+931A>G
XM_011510922.1:c.-64+931A>G XP_011509224.1:n.-64+931A>G
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