Canonical Allele Identifier: CA592356119
Gene: GAD2 HGNC NCBI

Linked Data

dbSNP Id: rs1410772018
gnomAD v2: 10-26505400-C-T
gnomAD v4: 10-26216471-C-T
MyVariant Identifiers: chr10:g.26505400C>T (hg19) chr10:g.26216471C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26216471C>T , CM000672.2:g.26216471C>T GRCh38
NC_000010.10:g.26505400C>T , CM000672.1:g.26505400C>T GRCh37
NC_000010.9:g.26545406C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376261.7:c.-339C>T ENSP00000365437.3:n.-339C>T
NM_000818.2:c.-339C>T NP_000809.1:n.-339C>T
NM_001134366.1:c.-339C>T NP_001127838.1:n.-339C>T
NM_000818.3:c.-339C>T NP_000809.1:n.-339C>T
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